Therapeutic stem cell composition and stimulant, facilitator, accelerator, and synergizer thereof, growth factor, anti-inflammatory composition and uses thereof

ABSTRACT

The present invention relates to a non-invasive medical therapy and a composition for avoiding organ transplantation, or controlling biological rejection of transplanted organs, or treating organs under consideration for replacement by transplant, and otherwise treating aged, diseased and/or abnormal tissues and/or organs. More specifically, the non-invasive medical therapy involves administering to a patient an elemental nutritional feeding comprising a free amino acid profile simulating and/or replicating a targeted diseased or transplanted tissue and/or organ. The subject invention provides methods of inactivating reactive component epitopes of moieties pathogenic substances or producing immunogenic compositions containing pathogenic substances comprising contacting pathogenic substances, or compositions containing pathogenic substances, with super critical carbon dioxide or liquid nitrogen. Similar benefits are produced using high HLB surfactants also reducing carcinogenic factors. In various embodiments, the pathogenic reactive components, epitopes, moieties or substances are inactivated and processed into immunogenic compositions. The subject invention also provides oral mucosal delivery systems for the subject therapeutic compositions and/or medications, and/or vaccines that avert the need for parenteral administration in the medical and veterinary fields.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application 60/358,890, filed Feb. 22, 2002 and 60/350,119, filed Nov. 9, 2001 each of which is hereby incorporated by reference in its entirety, including all figures, references, tables, and formulae. This application is a continuation in part of U.S. patent application Ser. No. 09/611,857, filed Jul. 7, 2000, pending, which is a divisional of U.S. patent application Ser. No. 09/080,990, filed May 19, 1998, which is a continuation in part of U.S. patent application Ser. No. 09/058,469, filed Apr. 10, 1998, which is a continuation in part of U.S. patent application Ser. No. 09/058,430, filed Apr. 10, 1998, which is a continuation in part of U.S. patent application Ser. No. 08/591,503, filed Feb. 2, 1996, which is a continuation in part of U.S. patent application Ser. No. 08/100,905, filed Aug. 3, 1993. This application is also a continuation in part of U.S. patent application Ser. No. 09/731,608, filed Dec. 7, 2000, which is a continuation in part of U.S. patent application Ser. No. 09/332,690, filed Jun. 14, 1999, which is a continuation of U.S. Pat. No. 5,912,040, which is a national stage filing of PCT/US94/08795, filed Aug. 2, 1994, now abandoned. This application is also a continuation in part of U.S. patent application Ser. No. 09/639,859, filed Aug. 16, 2000, pending, which claims priority to U.S. Provisional Application 60/149,338, filed Aug. 17, 1999. Each of the above-referenced patents, patent applications, and provisional patent applications are hereby incorporated by reference in their entireties, including all figures, formulae, references, and tables.

DESCRIPTION OF THE INVENTION

The subject invention provides methods of inactivating pathogenic substances or producing immunogenic compositions containing pathogenic substances comprising contacting pathogenic substances, or compositions containing pathogenic substances, with super critical carbon dioxide or liquid nitrogen. In various embodiments, the pathogenic substances are inactivated and processed into immunogenic compositions.

Pathogenic substances for including in pathogenic compositions include microbial pathogens (e.g., pathogens of bacterial, prion, protozoan or viral origin). Alternatively, pathogenic compositions can contain pathogenic eukaryotic cells, such as cancerous, malignant, or tumorigenic cells. In another embodiment, pathogenic substances can be proteins, glycoproteins, lipoproteins, peptides, glycopeptides, lipopeptides, toxins, lipotoxins, lipopolysaccharides, carbohydrates, autoantigens, and/or tumor-specific antigens that cause pathogenic effects in individuals. Pathogenic substances may be attenuated microbial, fungal, yeast, protozoan, or viral (or viral-like prions) pathogens. Other embodiments provide for the inactivation of known live vaccine formulations typically used in current vaccination protocols. In yet other embodiments, virulent (non-attenuated) pathogenic organisms (e.g., microbial (fungal, yeast), viral, or protozoan pathogens) (or viral-like abnormal protein prion) are contacted with super critical carbon dioxide or liquid nitrogen and formulated into immunogenic compositions. In certain embodiments, the immunogenic compositions provide protective immunity upon administration to an individual. The subject methods are applicable to pathogenic substances of veterinary and human interest, including such problematic disease producing entities as the prion, e.g., a 30,000 molecular weight abnormal cell protein in neurons; abnormal beta pleated sheet isomer or isoform P_(R)P^(Sc), which acquired relative resistance to digestion with proteases (a diseased conformation charge from normal alpha helix isoform or alpha helix isomer P_(R)P^(c)).

Liquid nitrogen cryogenic grinding (as with chocolate liquor or of beef, the potential bearer “vector” of prion induced mad cow disease) will produce a spatial isomer without reactive pathogenic components of prion. Liquid nitrogen cryogenic grinding of beef would be useful for the production of hamburger meat of the world-wide hamburger industry.

This non-reactive component, 30 kilo dalton structural re-isomerization, can be confirmed by comparison of normal, abnormal, and/or treated products in immunologic, biochemical, and/or other prion identification techniques, including, but not limited to, (1) RIA (Radioimmunoassay), ELISA, and IgE inhibition studies; (2) crystallographic studies of protein, as well as of amylose and amylopectin crystals (iodine stained, visualized with polarizing microscopy looking for change or absence of crystals after liquid N₂ or super critical CO₂ treatment. The allergic antibody can be looked upon as an IgE testing reagent against bovine protein, including beef Allergic antibodies, in turn, can be used to distinguish between allergic reactions, prion-induced mad cow disease (bovine spongiform encephalitis (BSE)) and, from liquid nitrogen or supercritical fluid (such as CO₂) treated bovine protein (beef); (3) probe of protein structure using ultraviolet absorption and fluorescence property changes of protein using retinal binding as a test.

Contacting pathogenic substances, and compositions thereof, with liquid nitrogen or super critical carbon dioxide reduces or eliminates pathogenic effects of these substances and allows for their use in the formulation of immunogenic compositions. Compositions containing mixtures of two or more pathogenic substances can be treated with liquid nitrogen and/or super critical carbon dioxide and used in the formulation of immunogenic compositions.

The term “individual(s)” is defined as a single mammal or avian to which is administered a compound or composition according to the present invention. The mammal may be a rodent, for example a mouse or rat, pig, horse, ape, rabbit, goat, pig, cow, cat, dog, or human. Avian animals include, but are not limited to, chickens, pigeons, squab, turkeys. Alternatively, the compounds or compositions can be administered by way of animal or human food(s). In a preferred embodiment, the individual is a human.

The subject invention also provides methods of reducing the amount of low molecular weight pathogenic substances in a solution or composition comprising contacting the solution or composition with an ultrafiltration or filtration membrane that allows for low molecular weight substances to pass through the membrane filter while retaining other components above the filter. Low molecular weight pathogenic substances include toxins and other pathogenic substances such as prions. In some embodiments, the molecular weight cutoff for the filter is 1.0 kDa, 1.5 kDa, 2 kDa, 3.5 kDa, 10 kDa, or 20 kDa. Ultrafiltered compositions or solutions are substantially free of low molecular weight pathogenic substances. In some embodiments, the ultrafiltered compositions or solutions contain less than about 0.25 wt. % of low molecular weight pathogenic substances. Other embodiments provide for ultrafiltered solutions or compositions containing less than about 0.025 wt. % of low molecular weight pathogenic substances. Yet other embodiments provide ultrafiltered compositions or solutions containing no of low molecular weight pathogenic substances (i.e., 0.0 wt. %).

The subject invention also provides an immunopharmacologically engineered composition for reducing immunoinflammatory reactions commonly encountered with the use of cow's milk. The composition contains a tasteful milk (sheep's milk) that is produced utilizing specialized animal husbandry techniques applied to dairy sheep used throughout the world, such as Friesland sheep. The reactive antigenic factors responsible for the production of allergic diseases are reduced or excluded by excluding hypersensitizing cow's milk protein(s). This biologic process of elimination is functionally equivalent to inactivation of reactive pathogenic components by processing with liquid nitrogen or supercritical carbon dioxide or via processing by removing reactive pathogenic components such as, but not limited to, proteins by ultrafiltration with the option of replacement with nonreactive components. These non-reactive components include, but are not limited to, proteins designed to be free of reactive pathogenic components. Sheep are poor anti-human protein antibody producer compared to other animal, another protein ribosomal template reflection of non-reactive protein as found in sheep's milk.

These products are offered and assembled as molecular components of a cellular and tissue analog transduction and delivery system that signals cells and synergistically stimulates stem cell function. This pharmacodynamic function that the replication of normal tissue and in replacement of disease tissue (a function can provide for similar to normal tissue being replaced daily and/or turned over every two to three months). This is utilized in conjunction with the incorporation of anti-inflammatory activity and tissue healing factor(s) to be bonded, released, and function upon contact with the internal milieu of the patient. These biochemical components will signal the activity of replication and tissue repair healing in conjunction with anti-inflammatory activity. This signaling will induce automated robot-like therapeutic function and can be applied to problematic disease entities. It has been determined that sheep's milk and its products can serve as a concentrated source of L-amino acids and can be presented in a safe format, along with an equal percentage of sheep's milk protein, free of pathogenic reactive components of allergenicity to foreign protein.

Sheep's milk, human milk, goat's milk, and cow's milk, all contain lactose. Sheep's milk is 1% higher in lactose concentration than goat's milk or cow's milk; human milk is 1% higher in lactose than sheep's milk. As indicated below, about 99+% of tested subjects, intolerant of bovine milk, all tolerated lactose containing sheep's milk. Allergists expect milk substitutes not to be enjoyed and expect many complaints from patients. Unexpectedly, more than 80-83% of study participants experienced therapeutic benefit upon the substitution of sheep's milk for cow's milk. These individuals also expressed a preference for, and enjoyment of, sheep's milk.

It has been stressed in U.S. provisional patent application Ser. No. 60/149,338, hereby incorporated by reference in its entirety, that microorganisms, bacterial, and microorganisms (bacterial, viral, yeast, and fingi), microorganism derived metabolic products, as well as microorganism-like prions can act as bacterial hypersensitizers in producing allergic disease along with their infections potentiating disease factors. Milk has yet to be shown to transmit the causative agent of BSE to humans or another consumer of the milk.

Another potential cause of allergic response can be eliminated by using the by-product permeates of mammalian milk and such productions as for cheese manufacturing. Disease spread by older animals, and who also have the lowest phospholipid content, suggest the elimination of older dairy cattle, e.g., lactating even at 20 years of age. It is the older animal that is susceptible to BSE. This subject therapeutic composition includes phospholipids such as phosphatidylcholine in treating this deficiency of aging.

It is noteworthy observation that dairy sheep farms in the above study do not have silos. That is because ensilage eaten by sheep would bring about an infection such as, but not limited to, clostridial or listeria, apparently not a concern in dairy cattle. However, up to 40 percent of dairy cattle had been observed to have ileitis (Johne's Disease in ruminants) and have to be sacrificed yearly. Johne's Disease might possibly correspond to the ingestion of ensilage with fermenting aging corn husks and as in humans might also be characterized by high levels of serum antibodies to brewers and baker's yeast (Saccharomyces cerevisiae). Humans with ileitis (Crohn's Disease, the human equivalent to Johne's Disease, is characterized by high levels of serum antibodies to brewers and baker's yeast (Saccharomyces cerevisiae) and Disease) are also highly allergically intolerant to cow's milk. Sheep and goats only have a one percent incidence of ileitis (Johne's Disease). Sheep's milk offers the highest percentage of butyric acid fats, helpful in healing inflamed intestines as in ileitis.

Sheep's milk has high butyric acid content. Sheep's milk contains about 2% more butyric acid than cow's milk (about 5.5% vs. 3.5%) Butyric acid levels are believed to be helpful in healing Crohn's Disease. Ammoniated butyric acid is valine. I have also found that another short chain deaminated aliphatic L amino acid 2 carbon 50% acetic acid will dramatically reverse long-term dermatitis and, fungal infection of the toe nail, even with significant damage to the nail, following brief periods of application of the acetic acid. The acetic acid represents the deaminated glycine in this subject composition can be applied one to seven days per week and can be applied, multiple times in one day. The duration of application can range from 2 to 60 minutes (or any other chosen interval) per application. This treatment protocol is particularly useful in patients allergic to standard anti-fungal agents used in the treatment of fungal infections.

Sheep's milk also contains significant amounts of amino acids useful in the manufacture of yogurt by bacteria, such as, but not limited to, Lactobacillus spp. Additional amino acids are also produced in yogurt production. As a result, most Crohn's Disease patients intolerant to cow's milk, tolerate and benefit from dairy products produced from sheep's milk, such as yogurts, sheep's milk, and yogurt ice creams and yogurt ice creams or yogurts produced from cow's milk. Thus, the subject invention provides compositions suitable for the treatment of gastrointestinal disorders, such as ileitis, milk allergy, Crohn's Disease, and IBD (inflammatory bowel disease), comprising the administration of sheep's milk or dairy products derived therefrom.

I have found that patients with milk allergies, milk intolerance and inflammatory bowel disease (IBD), such as ileitis (Crohn's Disease), tolerate yogurt much better. This conforms to the present invention in that yogurt has free amino acids of tyrosine, phenylalanine, and leucine, which constitutes more than half of the amino acids present; proline is also present. S. thermophilus peptidase initiates the proteolysis of casein. The greatest amount of free amino acid is produced with an equal bacterial amount (1:1 ratio) of Lactobacillus bulgaricus, concurrent with incubation and cooling. Therapeutic benefit is also derived from the anti-inflammatory healing effects of essential fatty acids (e.g., omega 3 and omega 6), via production of anti-inflammatory prostaglandins PG1 and PG3 (without stimulus for production of inflammatory protoglandins PG2); also, avoidance of trans fatty acids which block delta 6 desaturase enzymes and inflammatory prostaglandins provides therapeutic benefit. Thus, compositions for the treatment of milk allergies, milk intolerance, and IBD can also contain essential fatty acid fats. The monounsaturated fat in olive oil is very resistant to oxidation, and is useful in preventing free radical oxidation and initiating inflammatory prostaglandins.

The gastrointestinal healing effect of medium chain triglycerides (C6-C12) in coconut oil (also, natural-butyric C4 acid); a fraction of butter (advantageously, butter that is hypoallergenic) can also be added to further this healing effect. Additionally, medium and short chain fatty acids, independent of liver involvement in processing long chain fats and fat storage, can be added as a quick energy source, and are also somewhat water soluble increasing hydrophillic state and HLB.

The subject invention, in addition to the therapeutic component stressed here, also provides for the correction of abnormal blood levels of nutritional factors; (e.g., amino acids, essential fatty acids, mucopolysaccharides, vitamins, and minerals); these abnormalities may be due entirely to disease and complications (e.g., gastrointestinal loss of nutrients in illustration of ileitis), and risk factors of long term medications, such as corticosteroids, and prior poor nutritional habits including trans fatty acids (s in oleomargarine), which block enzymes, such as delta 6 desaturase, to produce anti-inflammatory prostoglandins (in contrast to most inflammatory PG2) and add to arteriosclerosis.

It would be advantageous to employ computer software, produced by the pharmaceutical companies developing these products, that can further individualize and maximize actions in production of elemental free L amino acid rich formulation analogs to normal tissue now diseased tissues. These formulations are specifically made for a multiplicity of severe illnesses, acute and chronic manifestations, and morbidity, mortality, and risks of medication that must be carefully considered along with severity of illness and achievable therapeutic benefits, in contrast to a therapeutic trial of free L amino acid low risk elemental formulations in the context of this invention.

In the aging process, where the production of digestive enzymes (to make free L amino acids) and growth hormone are diminished, the free amino acids of the inventive non-invasive therapeutic composition are anabolic and stimulate production of growth hormones, both of which are beneficial. Thus, the subject invention provides methods of treating conditions or symptoms associated with aging comprising the administration of compositions taught herein.

Sheep's milk contains (w/w) greater than about 5% amino acid. When all twenty amino acids are considered, the percentage is in excess of 6% (w/w). Sheep's milk, at 7% fat (and containing a significant percentage of short and medium chain fatty acids), has the highest levels of fat of domestic mammalian milks. This is important in healing diseases, such as the chronic granulomatous illeal lesions of Crohn's Disease, and possibly keeping the bowel surface normal with and minimizing or avoiding the uptake of allergenic food protein. This can also minimize food sensitization and food allergy.

The subject invention also provides an oral delivery system, chylomicron mediated, with special application to vaccine administration. This oral delivery system is also useful for the delivery of other orally administered drugs, such as insulin.

The oral delivery system of the invention comprises a chylomicron vehicle, typically of 0.5 to 1 micron in size. The chylomicrons can be made according to methods well known in the art. By way of example, one component comprises palm kernel oil and coconut oil. This component comprises ⅔ of the composition and contains 40% palm kernel oil and 60% coconut oil. The other ⅓ of the composition comprises corn oil. These materials are mixed together and warmed to approximately 110-120° F. 100 ml of the liquid fat is combined with one or more surfactants and the mixture is used to suspend an antigen or drug. Surfactants useful in this aspect of the invention include PGPR (polyglycerol polyricinolate; 0.3% of the final product), PC (phosphatidylcholine; 0.15 percent of final product), glycerine (U.S.P. 0.5 percent of final product), and Tween 80 (polysorbate 80; 0.3 to 0.5 percent of final product). The final liquified suspension can be emulsified with the use of a homogenizer, e.g., Manton Gaulin 3 to 8000 psi instantaneous processing, and was emulsified by a colloid mill. The particles' size was in sample production and can be confirmed by microscopy and can be between about ½ and about 1 micron in size using size standards known in the art. For example, the oral delivery system described above has been used to deliver urease, an antigen not encountered by poultry to poultry (provided at 50 mg/pound). A soft fat can be used to permit prolonged residence, in the oral cavity, for oral mucosal absorption. Antigen delivered via this system induced an antibody response equivalent to that produce by standard injection of antigen. By feeding the antigen delivery system described herein after fasting chickens for 2 hours (chicken store ingestants in gullet for prolonged time as a fasting defense), antibody level was equal to injectable response. This also appears to be an additional breakthrough in acquisition of oral tolerance (not usually seen in avian species as chickens).

Sheep's milk can also be augmented and extended to cover other bacteria, sheep could serve as a convalescent serum or a low allergenicity therapeutic composition.

The oral delivery system can also be mixed with flavoraids, such as those described in U.S. Pat. Nos. 6,197,356; 5,912,040; and 5,753,296, and provisional application Ser. No. 60/149,338, each of which is hereby incorporated by reference in its entirety. Chocolate, white chocolate free of caffeine and theobromine, can be used to incorporate a synergistic flavoring and savoring mechanism delivery system to maximize mucous membrane absorption. An ideal delivery system for a medication such as a specifically prepared stem cell stimulant anti-inflammatory stem cell and tissue healing therapeutic agent is included in one of the embodiments. Here the sheep milk with six percent free L amino acids may optionally constitute the milk composition of milk chocolate. L amino acid concentrations can be further heightened by probiotic yogurt treatment which would enhance the level of amino acids even further. Also useful for the delivery of vitamins and minerals, it has been noted that the dairy animals with the highest concentration of L amino acids in their milk have the highest body temperature. This enhances probiotic temperature of the heat loving or thermophilic microorganisms such as, but not limited to Streptococcus thermophilus, which is used in one-to-one concentrations in conjunction with Lactobacillus bulgaricus. The highest L amino acid concentrations are found in sheep and goat's milk (the highest in sheep's milk) with highest temperatures of about 102 degrees Fahrenheit rectal temperature. Human rectal temperature is 99.6° F. in contrast to bovine rectal temperatures of 101.5° F. The chicken's temperature is even higher at 107° Fahrenheit (rectal temperature).

A stem cell formulation based upon an extrapolation from a life model about the origin of life was a formation of the first cell, in which polymer chains of at the least two of three types now represented/used here by free L amino acids (an analog of human cellular tissue proteins), nucleic acids (DNA), proteins, and a semi-permeable membrane comprising phospholipids, lipoproteins, and glycoproteins which orient vesicle formation of a surrounding cell membrane. These vesicles can be further surrounded by extracellular matrix mucopolysaccharide.

I have found that the biochemical pathogenic reactive components appear in disease in many formats but can be exemplified in microorganisms and microorganism-like substances including virus and prions. The primary disease factor here seems to be the foreign proteins which include the lipoprotein, and lipopolysaccharide (LPS), the essence of the tuberculin test, as well as toxic shock disease and bacterial cell membranes (for Gram negative bacteria).

The proteins may be modified by extremes of biophysical processing such as temperature cracking (similar to the fractional distillation of petroleum). In the case of the protein polymer, the most hydrophobic (lipophilic) amino acid components are located within the center of the molecule. Differences in freezing points and melting points in the case of submerging for treatment with liquid nitrogen at a temperature of −320 degrees Fahrenheit place great stress upon the molecule with resultant cold denaturation and a 3-D configurational change in the spatial appearance of the molecule. Similar effects may be noted with supercritical carbon dioxide processing.

Natural processing of sheep's milk proteins results in a protein that does not require the above specialized food processing therapy, since our current study in 199 patients, who were allergically intolerant to cow's milk, showed this milk to be about 99 plus percent efficacious as a hypoallergenic substitute for cow's milk. Our current study shows a very high acceptance rate of about 83 percent for sheep's milk. This is in contrast to acceptance rates of 35 percent for other milk substitutes such as soy, and goat milk. Similar acceptance rates were seen with rice almond and oat substitutes. There was about 90 percent tolerance for goat's milk, and about 95 percent tolerance for soy milk; however, in the U.S. I have found poor success with goat's milk (as a cow's milk substitute). This may be due to the heat treatment or pasteurization of canned goat's milk which may alter it from its natural state or condition.

This naturally hypoallergenic protein is present at about six percent, and the amino acid “pre-protein” which also may be referred to as bioaminenergic or bioamine are available in a similar about six percent level in this especially available and prepared foods as the sheep's milk and to attain this level of hypoallergenicity the above additional processing is not necessary.

It is noteworthy, with the stem cell growth factor observed with L amino acids, that the sheep is the only animal where a successful clone has been biologically accomplished.

The naturally occurring endorphins, dynorphans, enkephalins family of endogenus morphine-like opioid compounds have 31 amino acids. The use of L amino acid analogue composition, comprising similar molar ratios of free L-amino acids to these 31 amino acids of 91 amino acid precursor polypeptide compounds, would be expected to have a similar analogue activity. Patients with narcotic drug addiction have lower blood levels of amino acids. This composition and it use would also obviate morphine side effect of enhancing the dissemination of cancer, as well as increasing prolactin which also enhances the dissemination of breast and prostrate cancer.

The use of hydrophilic surfactants with a high HLB approaching 20 such as Tween 80, phosphatidylcholine (PC) with an HLB of 13, as well as the L amino acids, and butyric acid compounds (the C6, 8, and C10 carbon fatty acid fats) would be expected to help kill bacteria, attack the protein lipopolysaccharide endotoxin of bacteria including the gram negative bacteria, to help enhance antibiotic sensitivity. Other compounds that have such activity also have a similarly lethal effect on cancers cells. The mode and rationale for discovery and use of heavy metal platinum (also bactericidal) in treatment in killing cancer cells. This has a high level of side effects. In addition, mitosis seems to also be incorporating and concentrating phospholipids such as PC of the cellular and nuclear membrane components in its genetic activity. Hydrophilic surfactants with high HLB of 18 Tween 80 polysorbate 80 (of 20=H₂O), and other hydrophilic surfactants which include sodium lauryl sulfate with a high HLB of 20, free of side effects, along with PC with HLB of 13; and seem to have effects of similar hydrophilic hydro-colloid activity that stimulates the reversal of mitosis. See Figures I, Ia, II, & III.

Figures I, Ia, II, and III are suggestive of similar biophysics: it was observed here, that the morphologies of mitosis were uniquely, highly similar to the biphasic diagram of hydrophobic reversed hexagonal biocolloid surfactant geometric patterns.

HLB effect is additive and use of PC, deficient in this aging population prone to cancer, would be important to include in HLB modulation. It seems likely that the overly reactive mitosis seen in cancer is the body's compensatory mechanism responsive to this PC and high HLB deficiency. Particularly in our current societal habit of excessive fat and sugar consumption without appropriate and proportionate hydrophilic HLB modulation. This PC deficiency may also better explain why cancer and atherosclerosis commonly occur, and occur together in this aging population and why atherosclerosis (including its effect in coronary disease) and other diseases of aging (e.g., arthritis, memory and mentation loss, onset of Type II diabetes mellitus, hypertension, and obesity associated with poor eating habits [excessive fat and sugar ingestion] and a sedentary lifestyle), would also be amenable to same hydrophilic HLB modulation.

It is likely that drugs such as, but not limited to, aspirin, particularly as used in this subject composition, are mediating their activity through some increase in HLB (through specially bonded formulations in these embodiments and subject composition or in internal milieu bonding in these embodiments and subject composition).

Yogurt like microorganism probiotic production probably accounts for this record amino acids level in that one of the highest levels was L amino acid, leucine 0.59 gram percent. The other L amino acids characteristic of (Streptococcus thermophilus) and Lactobacillus bulgaricus microorganisms of yogurt production phenylalanine, tyrosine and proline also were present in these milk products. Cyclosporin analog L amino acid in utility patent also are present: Glycine, valine, alanine, leucine and its isomer isoleucine as evidence of anti-rejection stem cell activity, without complication of rejection like allergic reactivity problematic in cow's milk, and goat's milk. Since the temperature of maximal function of lactobacillus is to 37 degrees to 45 degrees C., it is possible that the heat loss must be considerably less, and therefore possibly higher body temperature in the sheep (39 degrees+C.) with its uniquely characteristic insulated wool “coat” fostering greater lactobacillus L amino acid productive activity (rectal temperature 102° F.).

We are what we eat, and our food chain represents a similar reflection. This is best exemplified by the omega 3 EPA fatty acids of fish, whose production is dependent upon the ingestion of algae, which may not be present as a source of food for fish in a fish farm like program. Also, considerations applicable to natural biologic activity of subject composition sources of a stem cell stimulant therapeutic composition and medication.

It might be considered that the HLB number obviously has to be related to the surfactant parameter (V/al) which describes the actual geometry of the molecule. Consequently, the HLB-value may also be roughly estimated from studies of the solution properties of the emulsifier, which basically is a very simplified way to determine the phase diagram. In this way, qualitative information on how salt, sugar, pH, alcohol and temperature influence the effective HLB value of the surfactant can be obtained.

The relation between the aggregates formed, the geometrical shape of the spatial 3-D comparative proteins of milk production (performed by comparative protein crystallography), surfactant (and its manifestation), the macroscopic character, the HLB number, and the surfactant packing parameter. The macroscopic character refers to a 5% mixture of the surfactant in water (comparative Dü Nouy tensiometry and phospholipid lipoprotein glycoprotein concentrations are important).

A study of 206 individuals, 195 of whom were intolerant to cow's milk (11 were tolerant to cow's milk) demonstrated the advantageous nature of using sheep's milk for treatment of food allergies due to cow's milk, a common cause of food allergy, and symptoms associated therewith. These individuals listed other offensive dairy products (containing cow's milk) such as custard, chocolate, yogurt, milk puddings, butter, cheese, cream, and ice cream. Symptoms noted most frequently were diarrhea, nausea/vomiting, headache, irritability, stomach ache, bloating, skin rash, eczema, nasal congestion, migraine, hyperactivity (in childhood).

Of the 206 participants in the study, tolerance of sheep's milk was near unanimous; 99% tolerating sheep's milk with 83% preferring it. Other comparable milk substitutes, during the initial comparative trial period, gave responses preference to cow's milk of approximately 35%, leaving sheep's milk as the product most relied upon in this one year observation study. It is remarkable that the multiplicity and severity of allergic symptoms produced by cow's milk were relieved by the simplistic substitution of Sheep's milk. Other time honored comparative substitutes, (during the initial trial period for each participant), were much less satisfactory, averaging 35%. The presence (found in all mammalian milks) or absence (in non-animal milk substitutes) of lactose did not appear to be a factor. Additionally, it should be noted that commercially produced reduced lactose milks are treated with enzymes, such as lactase, and may have undergone modification of glycoproteins found in the milk when lactose is split off from the protein.

Cow's Milk Substitutes COW'S MILK SUBSTITUTES TOTAL SUBSTITUTE # PATIENTS TOLERATED PREFERRED Sheep 199 198 164 = 83% Soya 101 95  39 = 38.6% Goat 92 90  30 = 32.6% Rice 50 50  17 = 34% MISCELLANEOUS SUBSTITUTES TOLERATED PREFERRED Oats 11 3 Coconut 4 2 Almond 1 1 Clinical symptoms typically seen with cow's milk allergy include: 1 Colic to 3 months, 2 Eczema (asthma of the skin), 3 months to 3 years 3 Bronchial asthma, 2-3 years onward

Patient is admitted to the emergency room, age 20 with asthma; roll up sleeves and observe eczema. Possible lifetime stigma of cow's milk allergy. Stop milk and asthma can be relieved.

EXAMPLE II: Of a group of 73 participants (in total of 206), all now on sheep's milk, showing improvement of symptoms, 35 reported almost instant improvement of symptoms and 26 reported a gradual improvement of symptoms. Five reported a combination of instant and gradual improvement of symptoms. Incomplete answers were provided by 7 participants.

Most common other offending foods (other than dairy which was 100%) were chocolate 79 (of 133), wheat 37 (of 133), and beef 30 (of 133). Four breast feeding mothers noted the disappearance of their infant's colic, almost instantly, when the mothers discontinued ingestion of cow's milk and dairy products, and used sheep's milk as a substitute (emphasizing how milk can be a vector for foreign proteins ingested by a lactating mother, either human or animal [e.g., cows]). I have also been able to alleviate symptoms associated with arthritis and joint pain by eliminating milk (cow's milk) and beef from the diet of subject. This observation has been extended to other chronic arthritis patients (i.e., the elimination of cow's milk or beef from their diets. This observation can be used to salvage large numbers of patients that require joint replacement.

More Specific Diagnoses (133 of the Participants)

Eczema/Rash29

Diarrhea 29

Irritable Bowel 15

(includes colitis and Crohn's Disease)

Arthritis/Joint Pain 21

Asthma 21

(includes breathing problems)

Migraine 18

Dyslexia 9

Detecting causal factors of dyslexia can be illustrated as follows: Two brothers whose parent, a teacher, noticed changes in behavior after the ingestion of milk further noted changes in handwriting after the ingestion of milk or milk products. By daily charting of handwriting it was possible to note the deviation from diet correlating with behavioral changes and induced learning disabilities. One child became dyslexic and the other child developed phonetic spelling (manifested in the reversal of the letter L (to J) and 9 (to P)) and could not follow the lines on the page.

The art and science of chocolate manufacture continued to be dependent on a very labor intensive and training and technological know how of the conching process, time and temperature of lipid, phospholipid, and emulsifier complex chemistry with this sophisticated technology and expensive equipment for conching that is available to primarily, the very few but very large, multinational chocolate companies. It is not known that PGPR can reduce conching time of non Newtonian chocolate by reducing or overcoming inertia biochemically and biophysically, whereas, it is primarily and essentially mechanically as in the case of the conching of chocolate.

This invention makes possible for other companies with very limited, if any, chocolate conching facilities to receive chocolate shipped in a 40,000 pound tanker or as 5 to 10 lb. blocks into a very large melter tank (e.g., 2,000 pounds) and by adding an agitator or recirculator along with 0.3% PGPR (similar concentration of lecithin added 0.3 percent) this combined effect of several hours or more and mixing would bring about the flavor development of the best grade chocolate, whereas the time-honored technique of adding emulsifier and/or surfactants has been confined to the highly expensive labor-intensive conch.

A great economic saving and improvement in quality would result with net decreasing: (1) conching time concomitant with (2) the dependency on expensive cocoa butter for functionality of hollow molding, molding and demolding, (3) varieties of sourced products to meet marketing needs versus one base product with the only adjusted variable being PGPR, (4) the need for increased particle size to 50 microns at a sacrifice of good mouth feel, good taste, and good eating qualities. Regardless of which of these goals is desired, all result when melting is performed on a conched shipment of chocolate to such intermediate size companies in preparation for final use.

I have unexpectedly, and repeatedly, observed a dramatic reduction in viscosity when the last ½ of lecithin is routinely added to this very viscous chocolate 1/2 hour prior to completion and prior to beginning to conch. This observation has been made in all types of conches, Frisse, McIntyre, Ball.

Within a short period of time, the chocolate suddenly becomes very liquid without this viscosity reduction and sloshes about the conch for a definitive and finite time of only a few minutes. Then, most of this dramatic viscosity reduction is lost forever in this product.

This same, but more lasting, observation has been made with a highly efficient emulsifier surfactant PGPR (polyglyceryl polyrininoleate) and an improved version of PGPR (0.3 percent), available commercially. It is not known to the art that this same entity can be observed with PGPR. This same liquifying viscosity reduction effect lasts several hours even days and can be used to minimize the need for conching and the need for adding additional costly cocoa butter to chocolate for 70 to 90 (85 MacMichael hollow molding chocolate). It has been observed that 6% more cocoa butter is required when PGPR has not been added to the material (28-29% with PGPR versus 34% or more cocoa butter added without PGPR). Plastic molds must be used, for molding and enrobing chocolate, chocolate viscosity adjustment to 120-140 MacMichael permits the company to derive from one order of good quality 190 MacMichael (20 micron 28-29% cocoa butter fat chocolate) and with the addition of 0.3% PGPR to several thousand-pound batches of chocolate pre-made by a supplier and produced very good quality Standard of identity chocolate with finess of 20 microns (vs. 50 micron . . . fair quality chocolate [produced with 35-35% cocoa butter fat] and both produce 70 to 90 MacMichael viscosity chocolate simplifying plant production. Only one type of base chocolate is required by adding less PGPR (e.g., only 0.15% enrobing or molding chocolate will result in adapting to many orders) and can be tested as Standard in a MacMichael viscometor.

Once a chocolate sets with this PGPR (0.3% or 0.15%) dosage, the lowered viscosity functionality workability of 70 to 90 MacMichael is partially lost. In that remelting after 3-4 months of storage provides a viscosity of 120 is still a significant improvement over the original viscosity of 190 to 200 MacMichael, and has retained most factory functionality of enrobing and molding.

The viscosity of PGPR is increased to 0.5 percent, or even to one percent, the viscosity is progressively decreased so that hollow molding chocolate will allow the presence of more medication as in the above embodiment without disturbing viscosity in regard to pipe flow in the factory. Also, an equal amount of dry blend of sugar and cocoa (may also be processed with ambient gas as in this embodiment). This one percent PGPR chocolate would be functioning tantamount to a chocolate super solvent and a standard identity chocolate or a technically simpler compound coating chocolate (not requiring tempering) simplifying the steps of providing the above embodiments without the tedious, technical skill, labor-intensive requirement of conching. Such one percent PGPR chocolate composition would result in a reduction of fat from 28-29 percent to 14 to 15 percent with the option of adding 1-2 percent Salatrim fat to nutritionally further reduce calories from fat by another percentage as well as protecting the chocolate when shipped in terms of resistance to melting that I have unexpectedly observed. Enrobed salatrim chocolate is several times more resistant to melting with all day exposure to an 100 to 120° Fahrenheit temperature. When returned to an air conditioned temperature of 76° F., the somewhat softened chocolate returned to its prior molded state. Non-salatrim chocolates did not return to their prior molded format and fat separation (bloom occurred).

Another vehicle to dispense the therapeutic stem cell composition is in the form of an instant soda fountain chocolate soda using supercritical fluids, such as CO₂, or liquid Nitrogen treated cocoa or chocolate. The treated chocolate/cocoa is cryogenically ground and can be flavored with a natural or artificial flavor, such as citric acid, cherry, orange, grape, banana, chocolate cream, or other flavors. Vanilla (0.1% to 0.15% total [volume to volume]) and/or granulated sugar can also be added. Other sweeteners such as saccharin, aspartame, or other known sugar substitute sweeteners can be used if lower sugar content is desired. The addition of 6-8 ounces of seltzer or soda water to these vehicles results in a flavorful product suitable for the administration of medication. These vehicles are used to pleasantly deliver medications to pediatric or geriatric patients.

The subject application also provides, as a functional biochemical composition, primordial biochemical components of progenitor cells and tissue comprising:

a) one or more cell membrane components, such as phosphatidylcholine (a biophysical membrane cell membrane formative factor with intrinsic predisposition to cell membrane vesiculative formation, and also a very efficient delivery system) or other known phospholipid/fatty acid/sterol components;

b) L-amino acids (free) that enable reversible healing of damaged tissue—and/or excellent graft and/or organ acceptance (if not otherwise preventable by the synergistic use of a and c); and

c) one or more extracellular matrix mucopolysaccharide compositions (to further support progenitor stem cells which can, optionally, be additionally latticed/scaffolded with mucopolysaccharide for in vitro or in vivo use).

If required, the heart valve vascular lattice can be supplemented with the embryologic structure and biochemical components of umbilical cord(s), including, but not limited to, mucopolysaccharide and surfactant components including, but not limited to, phospholipids, sphingomyelin, sphingolipids, glycosphingolipids, gangliosides (such as those gangliosides which are primarily located on the outside surface of mammalian cell plasma membranes and responsible for cellular and intercellular adhesion, differentiation, and migration mechanisms). Their components include fatty acids mainly stearic, hexoses of glucose and/or galactose, L galactosamine, and sialic acid. Cell signaling may be utilized in valvular and vascular cell culture and grafting as exemplified by the anti-prostaglandin affect of aspirin in the correction of a patent ductus arteriosus. If other congenital heart defects are present, such as an obstructed pulmonary or aortic valvular system, patent ductus arteriosus may be maintained by the administration of prostaglandin E (the functional anti-thesis of aspirin). Similar cell signaling treatment, as incorporated in this subject composition, in conjunction with medication such as, but not limited to, aspirin or specially bonded medication in these embodiments, e.g., but not limited to, aspirin or internal milieu bonded compounds associated with the use of subject composition, may be utilized in the management of congenital heart disease in vitro, or in vivo.

Sialic acid residues and glycoprotein are the main cause of cell surface negative charge. Substances of elasmobranch origin derivatives (with high index of acceptance and readily established oral tolerance) can be added to heart valve and vascular structures and may also be included if required.

The earliest primordial origin of these components, even prior to stem cell differentiation, can be exemplified by plant thallophyte differentiation into stem, leaf, and root and might be referred to as a merocyte or stalk (in contrast to the differentiated stem) cell biochemical component.

These foregoing components, in the practice and medicine and pediatrics, can be looked upon as potentially rejection resistant and are not subject to hypersensitivity reactions. In fact, protection can be further reinforced by a unique oral tolerance mechanism.

The subject composition and its stimulant action in cell signaling can be used therapeutically in conjunction with other medication (and particularly synergistically with other medications to therapeutically add to maintenance, repair, and reversal to normal of cellular membrane leaks and damage to cell membrane involved in the pathogenesis of disease. This adds, to the patient's damaged cells and cellular debris, building blocks for reconstitution of the cell. The destruction of cell membrane and extracellular matrix is the modus operandi of a spectrum of various diseases (such as bacterial or viral infection and degenerative diseases (which include diseases of aging, arthritis (osteoarthritis), rheumatoid arthritis, lupus autoimmune damage, arteriosclerosis, coronary artery disease, diabetes, mellitus, hypertension, Alzheimer's disease, as well as all the compendium of diseases including, but not limited to, that found in the reading medical, pediatric, and immunologic texts)).

Additional available methyl groups can be derived from phosphatidylcholine to counter any homocystine or homocysteine predisposition that might aggravate the inflammation present in the pathophysiology of atherosclerosis and coronary artery disease.

The concurrent addition of this subject composition or any of its components to medications additionally furthers synergism by countering the long and the short-term toxicity, side effects and/or metabolic risks of such drugs and therapeutic agents such as, but not limited to, aspirin and nonsteroidal anti-inflammatory drugs in treatment protocols. Specifically, aspirin reduces phospholipids such as phosphatidylcholine along with reducing the cell life, e.g., of the erythrocyte.

The subject compositions are also useful in countering disease by providing barriers to the spread of infection, inflammation and metastasis of cancer (such as the mucopolysaccharide basement effect membrane so helpful in countering the metastasis of cancer). All tissues and organs requiring normal mucopolysaccharide basement membranes, as well as mucopolysaccharide integrin, and cadherin offering cell adherent function, as well as immunologic protective effect in antibody associated cellular immunity can benefit from the compositions of the subject invention.

This foregoing significant pharmaceutical synergism (with utilization and co-utilization of said therapeutic composition) is further synergized by its component lipid and phospholipid, such as phosphatidylcholine. Surfactant delivery systems, enhancing the dissemination of these therapeutic pharmaceutical components, as well as the subject composition also synergize the subject compositions.

This subject composition and/or its components can be further synergized by chemically bonding reactive chemical groups such as, for example, the acid carboxyl group in such treatment medications as aspirin, by esterification of lysolecithin (biochemically formed by the phospholipase A2 deacylation treatment of such surfactant lipid-phospholipids as phosphatidylcholine exposing the alcohol OH group or sulfasalazine (already bonded to aspirin) resulting in a pharmacodynamic small molecule that may be better utilized alone or in conjunction with the therapeutic composition of the subject invention. In the ester formation, water was split out, concurrent with the bonding of an alcohol with an acid group, in the present of a catalyst, such as nickel or zinc, which, of course, is usually removed at the completion of processing. The selection of aspirin, for example, as a bonding moiety synergistically adds its pharmacologic anti-inflammatory, analgesic, anti-atheromatous clot formation, anti-cancer activities to the chemical composition of the subject invention. Therapeutic compounds, such as aspirin, can also be bonded to mucopolysaccharides, collagen, cartilage, and/or chondroitin sulfate through available hydroxyl groups. This bonding can also be a peptide bonding, e.g., the acetyl group of aspirin to the NH₂ group of e.g. glucosamine. An added synergistic feature—In the case of arthritis, these chemical bondings to these mucopolysaccharides offer an added tropism and affinity to the inflamed arthritic joints.

The alcohol group in sphingosine of sphingomyelin or the glycosphingolipids (as well as the carbohydrate such as the OH on the glucose group) could also be available for these chemical bonding opportunities in the preparation of therapeutic agents.

An anti-inflammatory variant of the essential fatty acid linoleic acid can also be provided in the subject composition.

The extreme reactivity of double bonds, for example, the essential fatty acid fats, linoleic acid and linolenic acid, in this subject composition and particularly the isomer, conjugated linoleic acid can be further utilized here alone or in combination with the subject composition, by chemically bonding the acid acetyl or COOH group of aspirin to further augment this anti-inflammatory activity of aspirin and conjugated linoleic acid reactions.

This strategy can be expanded further by bonding pharmaceuticals (such as, but not limited to, aspirin to procaryote surfactant phospholipids unique to microorganisms). Procaryotic surfactant phospholipids include, but are not limited to, phosphatidylethanolamine, phosphatidylglycerol, and cardiolipin 1,3diphosphatidyl glycerol with one free hydroxyl group available for further bonding in anti-inflammatory therapy formulation. Further variations that would intensify the pharmacodynamic therapeutic effects and actions of these chemically bonded biochemicals would include further etherification of the chemically bonded compounds, or, in turn, esterification of the chemically bonded ether compounds. In addition, the esters of these pharmaceutical compounds can be further esterified; and the ethers of these pharmaceutical compounds could be further etherified.

Chemical bonding to a carbohydrate, instead of, a glycerol compound can enhance the pharmaceutical compound's hydrophilic polar head, lubricity, and an affinity for the outer plasma membrane surface. Exemplary carbohydrates include, but are not limited to, galactose, glucose, sorbitol, or polysaccharide, such as glucuronic sulfated polysaccharide or glucosamine and mucopolysaccharides such as, but not limited to, glycosaminoglycanc polymers of glucosamine compounds. In these foregoing synthetic reactions, sulfuric acid, may be required for the ether compound formation or other well-known methods. The condensation of two alcohol groups in ether formation, may be performed by the use of ethylene oxide in that the ethyl group may ultimately become part of the ROR either linkage or other well-known methods. This pharmacodynamic activity may be applicable to the Type II diabetic where the insulin appears to be adequate, but not released from the beta islet cells. Additional adjustment of HLB (Hydrophilic Lipophilic Balance) may be all that is required therapeutically. These synthetic compounds add to the lubricant affect of glycolipids present in other embodiments.

The HLB of these formulations can be advantageously adjusted as described herein or according to the delivery system, described in 60/350,119, filed Nov. 9, 2001, herein incorporated by reference in its entirety. HLB surfactant adjustment components have, as embodiment, any surfactant, such as, but not limited to, hydrophilic surfactants, and have an additive effect and may be blended to more precisely adjust HLB.

The bonding system is similarly applicable to surfactant lipids and phospholipids found in micro-organisms, including, but not limited to, the viruses (such as HIV). The synergistic activity of the subject composition can also help to avert the negative nitrogen balance and weakness, so commonly seen in AIDS, and other diseases caused by microorganisms including, but not limited to microorganisms, such as fungi, yeast, spirochetes, and microorganisms like prions.

As described in above, inclusion of surfactants and the glycosphingolipids, cerebrosides, and the gangliosides can further synergize and the subject compositions as a dissemination delivery system, drug bonding system, prevention of untoward drug side effects and drug metabolic side effects, and also serve in an attempt to reverse such intractable neurologic diseases as spinal cord injury.

Case example: averting a major drug (corticosteroids) side effect.

This subject therapeutic composition was administered locally and systemically to an adult patient, on long term steroids for an unrelated condition, who sustained an extensive dermal and deep subcutaneous tissue trauma. Periodic examinations were made to check the progressive healing, during a six-month observation period. With this therapeutic regime, the wound has completely healed to the satisfaction of the plastic surgeon. The therapeutic regime included all the components and patent claims outlined in Ser. No. 09/639,859, filed Aug. 16, 2001, herein incorporated by reference in its entirety. In addition, the local therapeutic cited components (page 9) derived from the therapeutic regime to counteract the increased presence of collagenase enzyme were administered locally and directly to the wound in the form of retinoic acid Vitamin A applied concurrently with antibiotic bacitracin-zinc oxide ointment. Local treatment applied to adjacent tissue surrounding this deep wound included zinc oxide ointment and retinoic acid. In so augmenting this treatment, the plastic surgeon was pleased to find the planned skin graft could be cancelled. Vitamin A zinc, such as in the form of an acetate, may be used alone or preferably synergistically in combination or conjunction with at least 2 components (e.g., PC and L amino acid(s)) of subject composition (e.g., for respiratory infection or pharyngitis or impending upper respiratory infection) as an orally administered medication, or locally as a lozenge or administered as oral mucosal delivery system as presented here in an embodiment. The local lozenge application is similar to the local use application in an embodiment in wound care. Has been found to greatly diminish the need for antibiotics when used in several patients and in several occasions.

Case example: Greatly accelerating the healing process and averting major drug side effects.

Again utilizing the subject therapeutic regime and compositions, and adding to the local dermatologic therapy and a mucopolysaccharide cartilage skin cream (cartilage derived from bovine tracheal rings), the complete formulation (including amino acid human tissue analog formulation) was now in an adult patient, age 69, with recent traumatic contusion and edema involving the entire forearm. Recovery was observed to occur in five (5) days versus the expected recovery period of one to two (1-2) months. (In this case, with the long term use of steroids complicating the healing process, one would have anticipated a much slower recovery process, making this even more unexpectedly dramatic, hastening the recovery period, and thereby greatly reducing morbidity). The last observation made by the attending physician on Jul. 13, 2001 revealed complete healing of this contusion.

Functional advantages of beta endorphine over morphine include the following: does not cause addition nor an increase in prolactin; not associated with dissemination and metastasis of cancer, and effective in control of pain and shock.

The free L amino acid analog of the active grouping of beta endorphine (available as free L amino acids may be represented by 3 amino acids: one mole of tyrosine, one mole of phenylalanine, and two moles of glycine, also represent analog grouping in common with the enkephalins (met and leu). The free L amino acid analog of beta endorphine may be functionally represented by two moles of L tyrosine, three moles of glycine, three moles of L phenylalanine, one mole of methionine, three moles of L threonine, two moles of L serine, five moles of L lysine, one mole of L glutamine, one mole of L proline, two moles of L leucine, one mole of L valine, two moles of L asparagine, two moles of L alanine, two moles of isoleucine, one mole of glutamic acid (all the foregoing free L amino acids are in these subject compositions being made available as free L amino acid, per se, as a functional therapeutic agent or as a self-bonded for formulation).

Utilizing the above application technology of bonding medication such as, but not limited to, aspirin, e.g., and the reactive groupings of the L amino acids such as, but not limited to, the hydroxyl groups of tyrosine, serine, and threonine; the amine groups with particular reference to the di amine groups of L amino acids arginine and lysine, the carboxylic acid groupings with particular reference to the di carboxylic acid, aspartic acid, glutamic acid and the reactive sulfhydryl groupings of cysteine and cystine.

Similar healing and protein repair applicable in the therapeutic complex bonding of proteins in vivo and in vitro would include sodium stearyl lactolate and also include diacetyl tartaric acid esters of mono and di glycerides, compounds of well-established safety.

The biologic strategy of diseases can be illustrated by snake and bee venom and action of their destructive enzyme phospholipase A2. Other inflammatory products that also are released include, but are not limited to, phospholipid enzymatic breakdown product of phospholipid PAF (platelet activating factor). The therapeutic strategy includes not only supplying the replacement of the biochemical essence of cell membranes, such as, but not limited to, phosphatidylcholine (this replacement effect may occur within seconds or minutes), but also to make available (and to further synergistically incorporate) safe anti-phospholipase A2 medications into the subject compositions. Phospholipase A2 inhibitors such as milrinone (trade name Primacor), generic Enoximone (useful in countering the vascular collapse and impending death associated with meningococcal septicemia, meningitis, and adrenocortical hemorrhage).

Stem cell compositions, along with stem cell stimulant of U.S. Ser. No. 09/639,859, hereby incorporated by reference in its entirety, may be used in cell culture along with progenitor cells from the umbilical cord or other sources in combination with mucopolysaccharide extracellular matrix and cellular membranes to produce blood vessels (such as the aorta), heart valves, or other body components or organs.

The scaffold upon which the stem cell culture can be carried out includes the extracellular matrix mucopolysaccharides taught herein. Alternatively, mucopolysaccharide (such as cartilage, collagen, or chondroitin sulfate powder) can be impregnated onto synthetic scaffolding, such as, but not limited to, polytetrafluoroethylene, dacron, orlon, or nylon or biodegradable polymer fiber of, e.g., polyglycolic and polylactic acid grafting material (such as natural stem cell origin or synthetic cylindrical blood vessels). The above mucopolysaccharide used to impregnate the scaffold may have heparin (also an extracellular matrix component) chemically bonded or adherently attached to the mucopolysaccharide and, optionally, an antibiotic may also be physically adherently attached or chemically bonded. (When this mucopolysaccharide is given orally, 70% of the cartilage, collagen, chondroitin sulfate powder is absorbed undigested. This feature also should be applicable to specially bonded and adherent medications such as, but not limited to, heparin and/or an antibiotic.) Shark aorta and valves of the elasmobranch may also be utilized in view of the low rejection potential associated therewith. Such grafts may be treated with gluteraldehyde, an antiseptic that also complexes protein polymer.

Platelet Activating Factor (PAF), a naturally acetylated lysolecithin and other enzymatic (cyclooxygenase and leuco-oxygenase) products, can also be counteracted by plant and fish oil omega-3 fatty acid fats. These beneficial effects may be augmented by plankton and algae of the sea so that the patient may produce these omega-3 fats. Aspirin and other nonsteroidal inflammatory drugs can also be provided to counter prostaglandin mediated inflammation by counteracting the enzymatic biosynthesis of prostaglandins. Aspirin also blocks and reverses intestinal cancer production from bowel polyps.

Modulation of uncontrolled cell growth (e.g., cancer) may also be effected by HLB modulation and may also be synergistically incorporated with said therapeutic composition and stem cell compositions described herein. HLB containing compositions can also be formulated with other medications such as, but not limited to, aspirin.

The therapeutic modulation of mitosis (as applied to cancer, for example) may be performed in conjunction with the utility patent stem cell therapeutic composition to permit co-healing and cellular regrowth to restore the tissue and organ status to normal as in many embodiments. Alternatively, adjustment of HLB to hydrophilic range of about 13 to 20 may optionally be performed alone. The surface tension measured in dynes of energy per square centimeter may be calibrated with a tensiometer, such as the duNuoy tensiometer.

Each surfactant, hydrophilic in this case, with usual concentration 0.5 to 1.0 percent concentration, may be so measured and monitored in vitro in physiologic saline or tissue culture, or in vivo, in mammalian tissue undergoing treatment (control vs. therapeutic application).

Benchmark tests of the efficacy of 3-D protein processing technology include:

1. Polarizing microscopic examination for absence of Maltese Cross crystal characteristic of the processed 3D structure of starch granule, in sharp contrast to non-processed sample with intact starch granule;

2. Immunologic studies for protein identity, e.g., ELISA inhibition studies using the allergic patient's reactive to the native unprocessed protein, in contrast to the 3D processed protein;

3. Histamine release studies using allergic patient's white blood cells and serum with histamine release reactive to the native unprocessed protein (in contrast to the 3D processed protein);

4. Bradford test for 3-D transformation after 3-D protein processing reactive for newly-exposed aromatic amino acids (particularly tryptophan, tyrosine, and phenylalanine, less so for histidine); and

5. Tests and new specific tests for 3-D pathogenic protein processing of protein polypeptide with liquid nitrogen and/or supercritical CO₂. This processing may be reinforced with surfactant processing with hydrophilic surfactant and/or their additional blends such as, but not limited to, Tween 80.

Objective Goal:

Processing of animal dander (such as cat dander) illustrates the feasibility of treating a cat with Tween 80 solubilized in a 1 to 2 percent aqueous glycerine alcohol with a smooth petting cloth, sponge or chamoix to reduce the allergenicity of the family cat. The efficacy of this processing technology was exemplified by processing commercial testing solutions of cat dander with ten percent Tween 80 added to this testing extract by gently warming and mixing to enhance solubility.

The results of the protein and IgE, ELISA inhibition assays are presented in the table below and companion graph of in vitro basophile histamine release.

As described below, allergenic extracts derived from cat hair and cat pelt source materials were modified. The modified extracts yielded significantly higher values based on the Bradford dye binding in contrast to the control untreated cat hair and pelt. Similarly, significantly less histamine was released, using in vitro white blood cell basophiles from a cat allergic patient exposed to treated cat hair extract, as compared to histamine released when the allergic patient was exposed to the untreated control cat hair extract.

Standardized cat hair extract (laboratory code GTE 3) at 10,000 BAU/ml and non-standardized glycerinated cat pelt extract (laboratories) at 1:20 weight/volume were treated with Tween 80 hydrophilic surfactant for modification of cat protein 3D molecular spatial arrangement by processing modification resulting in reduction of allergenicity for processing modification. The unmodified extracts were maintained at 2-8 degrees F.

Analytic Assays:

The protein comparisons of unmodified and modified extracts were determined using the Bradford protein assay using bovine serum albumin as the standard. Similar comparisons were made using the basophile histamine release in vitro assay from the white blood cells of a cat allergic patient.

Results:

The results of the proteins and IgE ELISA inhibition assays expressed as relative potency are presented in the table below, and demonstrates the 3-D processing effects of “straightening” of Protein (cat) polymer. This 3-D structural change of the allergenic cat hair protein molecule prevents or reduces the severity of the allergic disease. Bradford Protein Consent IgE Extract (mg/mL) ELISA Cat Hair - 11.70 0.906 Modified Cat Hair - 0.16 1.000 Control Cat Pelt - 34.60 0.375 Modified Cat Pelt - 0.72 1.000 Control

Documented are similar (100-250×) decreases in allergenicity using supercritical CO₂ processing of allergen of foods. Similar comparisons were made using hereof reduction of allergenicity of reactive components of cat dander in the basophile histamine release assays from the white blood cells of a cat allergic patient. See FIG. 4.

On further review, using the above technique dispensed in a plastic spray pump bottle containing 98 to 99 percent polysorbate 80 such as Tween 80 and conforming to the composition of Tween 80®, starting with a concentration of 0.25% to 2% with diluent H₂O, 0.5 to 1 percent glycerine, a good emolient without HLB effect and 0.5 to 1 percent of any non-toxic alcohol, should bring about the above effects. HLB effect is additive, 0.5 to 1% P.C. (HLB of 13), 0.5 to 1% sodium lauryl sulfate HLB of 20, may be respectively added to further adjust ideal HLB to optimize hypoallergenic effect for various animals or pets, e.g., dog, cat, animal hair (dander), etc.

Thus, the subject invention provides methods of reducing the allergenicity of pet allergens (e.g., cat dander) comprising the application of a solution comprising (v/v) primarily polysorbate 80 such as Tween 80%, and conforming to the composition of Tween 80® and starting with a minimum concentration or strength of 0.25 to 2%; 0.1 to 50% (v/v) of an acceptable carrier, such as glycerine, and 0.1 to 50% of any non-toxic alcohol such as, but not limited to, ethel alcohol or isopropyl alcohol (v/v). In certain embodiments, the carrier and alcohol will be present in amounts of 0.1 to 5% (v/v), 0.3 to 3% (v/v), or 0.5 to 1% (v/v). Optionally, an aerosol can, with the addition of Freon (amount required to develop pressure) or other suitable propellant, tolerable and efficacious to animal application, should be used. May also be used to lessen allergenicity and threatened reaction in same fashion if exposed by contact or inhalation to an allergen, e.g., but not limited to, poison ivy plant or similarly lipophilic allergenic weed as ragweed pollen, mold spores, or allergenic animal dander. After washing exposed area with water as diluent until one can use a more specific wash of 0.25% to 2% hydrophilic surfactant (HLB 18) as Tween 80® or sodium lauryl sulfate (HLB 20).

In the case of inhalant exposure, after blowing the nose to blow out allergen, then wash nostrils with saline and same subject hydrophilic surfactant (hydrophilic surfactant may be combined in saline), as inhalant pump spray or aerosol. Respiratory allergy or respiratory infection may be complicated by sinusitis and loculated purulent debris including hydrophobic cell membrane surfactant, microorganism lipids, phospholipid, and lipoprotein polysaccharides may be relieved by lavage and drainage with same subject hydrophilic surfactant composition (also applicable for any focal area of pus).

Similar application of subject composition in systemic use of subject composition, with particular reference to specific component PC (HLB of 13) may be used to reduce adherent hydrophobic surfactant effect of blocked coronary artery.

To reduce the allergenicity of foods anywhere in the food chain, it is the same high HLB hydrophilic surfactant technology such as, but not limited to, Tween 80 and PC processing agents acceptable for food use, as used in other embodiments in processing foods to reduce allergenicity. May also be administered orally as an antidote to diminish allergenicity of an already ingested food as soon after ingestion as possible, starting with 0.25% to 2% solution of hydrophilic surfactant such as, but not limited to, Tween 80. Caution: a very concentrated solution of hydrophilic surfactant (HLB 13-20), such as, but not limited to, Tween 80 (HLB 18) might dehydrate the suspected allergen with reversal of HLB to a former more hydrophobic effect status, thereby reversing and cancelling this processing and therapeutic action.

The probiotic and prebiotic effect of the subject compositions can also be enhanced by, as well as being produced by, amino acids such as those found in red wine of the French, as well as yogurt of the Afghan and Kurdish people. Such amino acids are not found in the unfermented substrates of these foods (thereby accounting for dramatic disease protective factors that may be synergistically incorporated in all of the above products, while at the same time maintaining the low-risk enhanced benefit medication profile presented in these patent applications). The yogurt bacteria (the lactobacillus bulgaricus producing, the greater bulk of the amino acids than streptococcus thermophilus and complete their fermentation process in four hours) work synergistically with slower growing-probiotic bacteria with good intestinal adherence properties lactobacillus acidophilus and casei (producing lactic acid) bifidobacteria (producing acetic and lactic acid) produce butyric acid with its antimutagenic, anticarcinogenic, and anti-bacterial activity. Butyric acid can also reduce cholesterol.

When L amino acids of this composition, concurrent with parenteral feedings, are given intravenously along with nothing by mouth within 24 to 48 hours, the gastrointestinal mucous membranes atrophy. The trans-location of commensal microorganisms or creation of a food portal (by this commensal microorganism) by a creating permeability defects having been deprived of food, particularly nitrogenous food, seems to be the factor in changing this mutual commensal bacterial flora relationship to that of invading microorganisms. This mutual commensalism seems to explain the intact functional gastrointestinal mucosa and the importance in this subject composition in inflammatory bowel disease; changing bacterial flora due to antibiotics, gastrointestinal surgery, as well as the pharmacodynamic rationale for adding prebiotic and probiotic bacteria, along with enzymes, such as, but not limited to, the digestive enzymes, including amylase, pancreatin, pepsin, lipase, papain, bromelain to subject composition, in particular, as applied to inflammatory bowel disease. These synergistic additions to the subject composition have furthered the management of a Crohn's inflammatory bowel disease patient further minimizing flare-ups and the need for corticosteroid medication, also applicable to peptic ulcer now known to be mediated by Helicobacter pylori.

The microorganism, plant, and/or animal components of therapeutic stem cell composition of the subject invention have minimal if any, toxic potential (in contrast to synthetically derived pharmaceutical compounds (even those as relatively safe and time-honored as aspirin and its other non-steroidal anti-inflammatory group members)). In diseases associated with aging, aspirin is quite effective as an anti-platelet or anti-clotting agent for treating coronary artery, atherosclerotic, or heart disease. However, even the smallest pediatric, slow release, long acting Ecotrin aspirin (in the form of 81 milligram tablets administered every other day) can cause gastrointestinal symptoms, such as the activation of a peptic ulcer or bleeding.

Additionally, bleeding complications must be constantly surveilled and considered with drugs such as aspirin or NSAID. Aging is associated with catabolism and negative nitrogen balance. Aspirin may also be associated with negative nitrogen balance, thus raising another unwanted complication for disease management in the aging population. Aspirin may also increase the production of corticosteroids, which may also account for these potential side effect risks, as well as interference in healing.

Another use for the stem cell compositions of the subject invention is in the prevention of tissue and/or organ graft rejection or the treatment thereof. Sheep's milk, with its high amino acid content, as well as its equivalent protein concentration, has been shown, in over 99 percent of the cases, to be free of major rejection-like reactions (e.g., such as those associated with allergic hypersensitivity), and may be used synergistically with the foregoing stem cell therapeutic composition. The sheep, its tissue, and its milk, as used and reported here, do not have to be specially cloned to avoid rejection mechanisms. The Suffolk wool producing sheep primarily share the genetic predisposition to harbor the Scrapie prion in sharp contrast to the Friesland dairy sheep. A similar disease, Alzheimer's exhibit similar genetic predisposition (as a Scrapie prion disease) with a similar prion-like beta pleated sheet protein (versus normal alpha helix random coil 3-D protein and proteomics). I have noted that the absence of this rejection-like hypersensitivity reaction as shown with sheep's milk correlates with the sheep (in contrast to goat, horse, and cow, e.g.) lack of immunologic antibody response to human protein (exhibiting poor template reflective transcriptive antibody response to human protein).

It is an object of the invention to provide novel uses for whey permeate, which has heretofore been regarded as an unusable waste by-product of cheeses manufacturing. It is also an object of the invention to provide an electrolyte beverage based upon whey permeate, useful as a sports drink or as a therapeutic aid in the replacement of electrolytes lost through vomiting or diarrhea. Another object of the invention to provide a process for the preparation of whey-based electrolyte beverages. Yet another an object of the invention to provide substantially hypoallergenic milk products from dairy permeates, which have enhanced flavor and palatability. These and other objects of the invention will be apparent from the following description.

An electrolyte beverage is provided comprising a pasteurized whey permeate and one or more flavoring agents. The whey permeate component preferably has a milk protein content of not more than about 0.25 wt. %, more preferably not more than about 0.1 wt. %, most preferably not more than about 0.025 wt. %.

A process for preparing an electrolyte beverage is also provided. Whey is filtered to form a whey permeate. The whey permeate is collected and treated to arrest microbial activity in the permeate. The treatment occurs promptly before significant microbe-induced degradation has occurred in the permeate. The permeate is then flavored with one or more flavoring agents. Preferably, the step of filtration is through a filter having a molecular size exclusion of at least as low as about 20 kDa, more preferably at least as low as about 10 kDa. The protein content of the permeate is preferably no more than about 0.25 wt. %, more preferably no more than about 0.1 wt. %, most preferably no more than about 0.025 wt. %.

A process for preparing a substantially hypoallergenic milk product is provided. Milk or whey is filtered to form a dairy permeate containing no more than about 0.5 wt % milk protein. The permeate is collected and treated to arrest microbial activity in the permeate. The treatment occurs promptly before significant microbe-induced degradation has occurred in the permeate. A hypoallergenic component is then added, and optional hypoallergenic fat.

By “dairy permeate” is meant a liquid portion of milk or whey which is collected upon passage of milk or whey, or liquid fraction of milk or whey, through a filter having a molecular size exclusion sufficient to filter out at least about 99.5 wt % of milk proteins, such that the permeate is rendered substantially hypoallergenic. Preferably, the dairy permeate results milk or whey using a filter having a molecular size exclusion of at least as small as about 20 kDa.

“Milk permeate” means a dairy permeate from filtration of milk. “Whey permeate” means a dairy product from filtration of whey. By “milk” is meant not only whole milk, but also skim milk or any liquid component thereof. By “whey” is meant the milk component remaining after all or a substantial portion of the fat and casein contained are removed. All percentages expressed herein are weight percentages (wt. %), unless indicated otherwise.

Cheeses are made by adding the enzyme rennin (rennet extract), or a combination of rennin and acid (usually lactic acid produced by starter cultures), to coagulate milk. The curds are separated from the whey and processed into cheese. All cheeses require a period of time for ripening. Ripening is brought about by microbial agents including bacteria, molds and/or yeasts. The same microbes are present in the whey. Their action can continue the cheese making process in whey, even though the curd has been removed.

Following removal of curd, whey is filtered to remove protein. The permeate, while being substantially free of protein, is an inexpensive source of minerals and vitamins, particularly those minerals which are found in modern electrolyte beverages used for the replacement of electrolytes. The present invention provides for the effective commercial utilization of whey permeate, which would otherwise be discarded by cheese manufacturers, or sold for a few cents per pound.

Dairy permeate is obtained upon crude filtration of milk or whey, that is, filtration using a dairy filter or membrane having a molecular weight size exclusion of approximately 20 kDa or lower. Whey may be diluted at least about 20% with water during the cheese making process, prior to filtration. If the filtration process is running properly, the permeate will have a protein content of as low as about 0.025%, based upon the weight of the permeate. Inefficient filtration, such as through a worn filter membrane, may increase the protein concentration by an order of magnitude, i.e., to about 0.25 wt. %. The protein concentration may be maintained at 0.025 wt. % by frequent servicing or replacement of the filter membrane/filter. Moreover, the protein content of the permeate can be minimized by selecting a filter/membrane with a smaller size exclusion, e.g. a 10 kDA filter.

A typical filter element useful in generating permeate from whey or milk comprises a polyethersulfone spiral membrane (Deaal Ultrafilter ER 3840C) having an average selectivity of 0.01.mu. (nominal), a typical operating range of 20-145 psi, and a maximum pressure drop per membrane element of 60-65 psi. The usual ideal daily range of pressure is 20 psi back pressure and 80-85 psi feed pressure.

The filter should be suitably “primed” prior to use. This is accomplished by allowing whey (or milk) to pass through the filter for at least about 15 minutes before collecting any of the permeate. The pre-15-minute permeate should be discarded as it may contain proteins large enough to be considered allergenic. For a whey permeate, the completion of the priming period is signaled by establishment of a permeate flow equal to about 84% by volume of the whey volume before filtration. Successful priming is also indicated by establishment of a permeate flow which has only minimal cloudiness, compared to the unfiltered whey.

Regardless of the efficiency of the filtration, the permeate should not have a milk protein content of more than about 0.25 wt. %, preferably no more than about 0.1 wt. %. A properly functioning dairy filter of the type described above will produce a permeate having only 0.025% protein. Milk contains about 3.25% protein. Thus, the permeate contains only about 0.71% of the protein of milk.

Maintaining a very low protein concentration in the dairy permeate, and therefore in the beverage based thereon, is important to minimizing the allergenicity or the product. Electrolyte beverages are typically entirely protein-free, since they generally comprise nothing more than synthetic mixtures of mineral salts to which flavoring has been added. Thus, the consuming public has come to expect that electrolyte beverages are hypoallergenic. Where, as in the present invention, a good-tasting electrolyte beverage is derived from milk protein-containing raw materials, care must be taken to reduce the allergenicity of the product to an acceptable level, consistent with the expectation that an electrolyte beverage will not contain allergens. Whey permeate, while not being perfectly hypoallergenic, contains such little protein that its consumption by the majority of milk protein-allergic individuals will be tolerated. Veterinary chemicals and medications used in dairy husbandry generally bind protein. Thus, the elimination of protein from the whey permeate will also remove such chemicals and medications.

It has been found that to maintain palatability, the dairy permeate should be treated quickly after it is generated. Whey permeate, in particular, is much more susceptible to bacterial contamination than milk. The same bacteria responsible for fermenting milk curd into cheese is also present in whey, and hence the whey permeate. Should those bacteria be permitted to act on the whey permeate to a substantial degree, the permeate, and hence the beverages formed therefrom, will possess a “cheesy” off-taste. Thus, the permeate should be treated as soon as possible after its generation to arrest the activity of the cheese-making microbes therein. Treatment should occur before significant microbe-induced degradation of the permeate has taken place. The common cheesy odor of whey products is thereby eliminated.

The most common change in milk products resulting from the growth of microorganisms is the development of acid. The action of cheese-making bacteria on the dairy permeate, and whey permeate in particular, may be monitored as a drop in the pH of the permeate. The pH of the dairy permeate, which is typically about 6.2-6.4 (6.3 being the most usual value) immediately after the permeate is collected, will decline to about 6.2, and possibly lower, such as to 5.9, if the cheese-making bacteria remain unchecked. Thus, the dairy permeate should be treated before the pH of the permeate falls off significantly from 6.3. It has been observed that prompt treatment delays the onset of deterioration of the pH, titratable acidity, taste and smell by 3 or more hours at room temperature. Preferably, the permeate is treated to arrest the cheese-making microbes much before the pH of the permeate falls more than about 0.3 pH unit from the initial pH value at the time of collection. A fall in pH of this magnitude is associated with departure from a fresh milk-like taste. It has been found that a significant increase in microbial growth (about two-fold) will occur about 2 hours following permeate collection, at about room temperature. At about one hour there is no significant change in microbial growth. The least growth is seen at about 15 minutes post collection. Thus, it is preferred that the permeate is treated to arrest microbial growth within about 2 hours of the permeate's collection, more preferably within about 1 hour, most preferably within about 15 minutes. The permeate should be treated even sooner if the dairy plant is not located in a cool climate, or is not air conditioned. Thus, where possible, the permeate is treated immediately upon collection. Where the permeate is refrigerated after collection, the interval may be longer, as refrigeration will retard the action of the cheese-making microbes and preserve the flavor of the whey permeate for some time. If a dry powder is the goal, then immediate drying enhances the efficiency of energy utilized.

The treatment to arrest microbial activity is preferably coupled with permeate production in a continuous process. Accordingly, the permeate is continuously collected. The continuously collected permeate is continuously treated to arrest microbial activity. In this manner, the permeate is treated without the delay which would be attendant in batch production and processing.

The most effective treatment for arresting the action of microbes in the permeate comprises pasteurization. Pasteurization generally comprises partial sterilization at a temperature and for a period of time that destroys objectionable organisms, without major chemical alteration of the product. To arrest the activity of the cheese-making bacteria in the permeate, particularly whey permeate, pasteurization may comprise heating the permeate to a temperature of at least about 110° F., more preferably at least about 120° F., most preferably about 145° F., and maintaining that temperature for at least about 30 minutes with constant stirring, for example, stirring with an agitator at 60 rpm. According to the so-called “holding method”, the permeate may be heated to 145° F. and held at this temperature for 30 minutes with constant stirring with an agitator at 60 rpm. Alternatively, a high-temperature, short-time process (“batch pasteurization”) may be employed. The latter requires a temperature of 162° F. for 16 seconds. Even shorter duration processes (278° F. for 4-6 seconds, or 285° F. for 2 seconds) may be employed, but are not preferred because of the added expense. Any combination of time and temperature may be utilized so long as it achieves adequate pasteurization of the whey permeate to result in the arrest of microbial growth. The result is an excellent dairy taste which is maintained under refrigeration for three weeks. A taste panel of five individuals found the taste of refrigerated whey permeate to be bland but pleasant, and not salty.

The dairy permeate is essentially free of casein and lactalglobulin, which are removed in the filtration process. Lactalbumin, which is not removed in the filtration process, is the most heat labile of all proteins. It is readily denatured even by pasteurization conditions. Hence, the permeate is substantially hypoallergenic, even if some lactalbumin remains therein.

The dairy permeate, from which greater than 99% of the milk protein has been removed, is also essentially free of any veterinary or agricultural chemicals since protein comprises the principal binding sites for these chemicals.

The permeate may be rendered even more hypoallergenic by heat treatment at 145-155° F. with constant stirring for 24-48 hours, preferably 36 hours. Thus further heat treatment may have the advantage of further denaturing or destroying secondary structures of food antigens. In particular, the heat treatment will denature any lactalbumin which may remain in the permeate, although trace portions of this heat labile protein which has been treated for 30 minutes at 145° F., for the minimum essentials of batch pasteurization, will not have an effect on most allergic individuals.

Although the permeate, appropriately treated to arrest microbial growth, may be utilized in liquid form to prepare the beverages described herein, it may also be dried to a powder and later reconstituted. If a dried permeate powder is desired, the drying should take place promptly after the treatment to arrest microbial growth. This obviates the need for refrigeration of the powder.

The liquid permeate may be dried to a moisture content of about 4 wt. % by spray drying employing, for example, a dryer inlet temperature of 400° F. and a dryer outlet temperature of 200° F., a drying time of four to five hours, a pressure of 2000-2500 psi, and a 68-70 gauge spray nozzle bore. Suitable spray dryers are available from, for example, Delfab (Delaware, Ohio). Suitable spray nozzles are available, for example, from Spray Drying Systems (Wheaton, Ill.).

Alternatively, the liquid permeate may be concentrated to about 45 wt. % moisture in a suitable evaporator device, such as the devices available from Weegan (Logan, Utah). In subsequent spray drying to 4% moisture, the spray nozzle gauge should be increased to 60-62 gauge, in order to handle the thicker consistency of the evaporated permeate. Preferably, about 0.25% soy-oat powder is added to the permeate to promote drying. Drying by a belt-dryer may be substituted for spray drying. The dried powder may be optionally further heat treated at from about 145 to about 155° F., for from about 24 to about 48 hours, preferably about 36 hours.

The dried permeate powder may be reconstituted with water. Spring water or distilled water should be used to avoid the chlorine taste of tap water. The powder may be reconstituted by adding 95 wt. parts water to 5 wt. parts powder, for example.

To prepare a hypoallergenic milk product, the permeate (liquid or dried milk permeate or whey permeate) is supplemented with hypoallergenic protein and, optionally, fat, as set forth in U.S. Pat. No. 5,064,674 or 5,204,134, incorporated herein by reference. The hypoallergenic protein component may comprise hypoallergenic protein per se, such as protein from cereal or vegetable sources. Alternatively, or additionally, it may comprise free amino acids, or “short chain polypeptides” of animal source. By “short chain polypeptide” is meant a polypeptide having a molecular weight of not more than about 5 kDa, preferably not more than about 1.5 kDa, more preferable not more than about 1 kDa.

Sources of hypoallergenic protein include, but are not limited to: oat cereal (which has a high protein level of about 18%); rice cereal; barley cereal; or any other food source having a low allergenicity and ample protein content. Vegetable sources of protein may also be used, so long as they have a low allergenic potential. Vegetable sources of low allergenic protein include, for example, potato and soy isolate. Combinations of the foregoing proteins may also be used. Oat cereal, for example oatmeal, is preferred because it not only enhances the protein content, but also adds to the taste of the resulting product. The oat cereal is used as a very finely ground flour, to facilitate dissolution into the permeate. About 5 to 10 grams of the very finely ground and sieved cereal flour is added to about 100 cc of product. The resulting mixture has a protein content of about 0.9 to 1.8% by weight, which is similar to human breast milk.

When cereals are used, protein soy isolate may also be added to enrich the lysine amino acid value of the cereal. Additionally, the protein may be supplemented with, among other things, methionine, cystine, and iodine to meet the minimum daily requirements.

Protein soy isolate is preferred for use in hypoallergenic milk which is intended for infants who require a single source of protein, or children and adolescents with important growth factor requirements. Cereal hypoallergenic protein sources can be used in the hypoallergenic milk for adults. For example, if a multiple source of protein is desired, any combination of hypoallergenic protein sources may be used.

In lieu of, or in addition to, supplementation with hypoallergenic protein, the product may be supplemented with amino acids, short chain polypeptides, or a combination thereof. Free amino acids and short chain polypeptides are hypoallergenic regardless of source, and therefore will not contribute to the allergenicity of the milk product. Preferably, the amino acids comprise a mixture of amino acids, most preferably a mixture containing at least the nine amino acids which are essential to the human diet: Threonine Valine Phenylalanine Methionine Isoleucine Histidine Lysine Leucine Tryptopan

The short chain polypeptides may comprise individual polypeptides or a mixture of polypeptides. The short chain polypeptides and amino acids may be obtained by appropriate hydrolysis of any suitable polypeptides or proteins. Preferably, they are obtained from milk proteins, so that the reconstituted hypoallergenic milk product of the invention maintains a portion of the protein nutritional content of whole milk. Hydrolysates of milk proteins are commercially available, a highly hydrolyzed pancreatic digestive of casein. A hydrolyzed pancreatic digest of another milk protein, lactalbumin, may be utilized. High-performance liquid chromatography indicates that these products are free of polypeptides having a molecular weight of greater than about 1.5 kDa. Hydrolysates of non-milk proteins may also be employed, e.g., a papaic digest of soy flour.

The sources of the optional fat component may include deproteinized clear butter and butter oil or butter fat, polyunsaturated and mono- and/or polyunsaturated vegetable oil or fat from milk free margarine sources, sesame, safflower, and the like, or mixtures thereof. The foregoing fats are hypoallergenic.

Deproteinized hypoallergenic butter for supplementing the permeate may be made from commercially available salt-free, sweet 99.99% anhydrous milk fat. The milk fat is melted in boiling water. The resulting butter oil is then removed from the boiling water, such as by pipetting it off the surface of the water. The boiling water results in extreme heat denaturation of protein and also renders the resulting heat-denatured protein insoluble. The process removes, by dilution and washing of the milk fat with water, any protein which may be contained in the fat as a contaminant. The process may be repeated any number of times to ensure the purity of the resulting butter product. Vitamin E may be added to prevent oxidation.

The deproteinized hypoallergenic butter advantageously includes vitamin E as an antioxidant. Vitamins, and further minerals in addition to whose present in the permeate, are also optionally added to the protein and fat-supplemented permeate. Such vitamins and minerals are added, so that the resulting milk products meet the minimum daily requirement.

Whey permeate appropriately flavored with one or more flavoring agents, may be used as an electrolyte beverage. Pasteurized whey permeate will generally have a potassium concentration of about 37 mEq/L. While a such a high potassium level is tolerated by most individuals, it may be desirable to reduce the potassium level by diluting the permeate before use in formulating beverages, particularly electrolyte beverages. High potassium concentrations might be harmful to individuals suffering from kidney or cardiac disfunction, and may be undesirable even for normal individuals after extreme exercise. Thus, it may be advisable, particularly in the preparation of electrolyte beverages for consumption by patients with kidney function impairment, to reduce the potassium level of the permeate to about 30 mEq/L or lower, more preferably to about 25 mEq/L, or even lower. The diluent most advantageously comprises water. For use in compositions designed to be taken following extreme exercise, the permeate should be diluted about 1:10 or more, to provide a potassium concentration of no more than about 5 mEq/L, preferably no more than about 4 mEq/L, ideally no more than about 3 mEq/L.

Whey permeate which has been diluted with water, e.g., 2:1, to adjust the potassium concentration to a level appropriate for electrolyte therapy for fluid loss, is somewhat low in sodium. Whey permeate contains about 15 mEq/L sodium. Thus, it is appropriate to boost the sodium concentration of the whey permeate by adding sodium, such as in the form of sodium chloride and/or sodium citrate, particularly when the permeate is used as an electrolyte beverage. Other sodium salts may be substituted. The sodium concentration of the beverage is preferably boosted in this manner to at least about 45 mEq/L.

The approximate concentrations of other minerals in the whey permeate are as follows: calcium, 10 mEq/L; magnesium, 5 mEq/L; and phosphorus, 7 mEq/L.

The dairy permeate contains substantial amounts of carbohydrate, in the form of the disaccharide lactose. The enzyme lactase (.beta.-galactosidase) may be added to the beverage to break down lactose, in order to avert problems with consumption by lactose-intolerant individuals, and to promptly provide monosaccharides not dependent on disaccharide digestion. Approximately 15% of the population over the age of six years has been estimated to suffer from lactase deficiency. The amount of lactase added should be sufficient to substantially hydrolyze the lactose contained in the permeate into its component monosaccharides, galactose and glucose. The glucose contributes to the sweetening of the permeate.

Further dilutions and mineral adjustments may be incorporated as necessary to obtain a permeate product which is isotonic or isomolar with respect to the osmolarity of blood (300 milliosmoles/L).

Whey permeate is flavored with one or more flavoring agents for use as an electrolyte beverage. The flavoring agent may comprise virtually any agent suitable for flavoring beverages, compatible with the use of the beverage as an electrolyte replacement drink. The flavoring agent may advantageously comprise, for example, any of the following fruit flavors, derived from fruit concentrates of low allergic potential: lemon, lime, grapefruit, banana, pear, hypoallergenic chocolate, low-acid orange and blends thereof. Low-acid orange has been observed to be hypoallergenic. Pear is preferably heat-treated to further enhance hypoallergenicity. Vanilla, oat, and rice are other suitable flavors. Such flavoring agents are commercially available. The amount of flavoring agent added to the pasteurized permeate depends upon the strength of the particular agent and the desired taste. Typically, the beverage may comprise about 5 wt. % flavoring agent.

The resulting electrolyte beverage may be taken as a sports drink after vigorous exercise, to replace sweat. The beverage may also be used as a therapeutic drink, to replace gastrointestinal fluid and electrolytes lost from vomiting or diarrhea caused by gastroenteritis.

The electrolyte beverage may also be used as an “elemental” feeding, with the inclusion of appropriate additional ingredients, such as amino acids. Elemental feeding compositions will generally contain simple sugars such as glucose, amino acids and electrolytes. Such a feeding composition may be used for providing nourishment to post-operative patients, particularly post-operative bowel surgery patients. It also finds use in administering nourishment to patients suffering from bowel disorders or diseases, such as chronic ileitis or colitis. Amino acids may also be added in the case of a sports exercise drink, to stimulate the restoration of muscle tissue which may be lost through vigorous exercise.

When added to the electrolyte beverage, amino acids are present in the range of, for example, from about 0.5 to about 2.0 wt. %. Preferably, a mixture of amino acids is employed which contains no more than about 0.25% protein, preferably no more than about 0.1%, most preferably no more than about 0.025%.

Although derived from a milk product, i.e., milk or whey, the dairy permeate is substantially milk protein-free. The dairy permeate contains no more than about 0.25 wt %, more preferably no more than about 0.1 wt %, most preferably no more than about 0.025 wt %, milk protein. Thus, beverages utilizing the permeate may be enjoyed by mildly or moderately milk-allergic individuals.

To form a chocolate-flavored drink, the dairy permeate, and the whey permeate in particular, may be flavored with a cocoa powder. To maintain the reduced allergenicity of the product, only hypoallergenic chocolate flavorings are recommended, such as the heat-treated cocoa powder described in U.S. Pat. No. 4,078,093. As described therein, a hypoallergenic cocoa powder is prepared by heating ground nibs of cocoa beans at high temperature and pressure. Alternatively, the whey permeate may be flavored with the complete hypoallergenic chocolate described in U.S. Pat. No. 4,078,093, which is prepared by mixing the cocoa powder with sugar, cocoa butter and flavoring additives, followed by further heat treatment to produce a hypoallergenic chocolate.

Alternatively, the chocolate flavoring agent may comprise defatted cocoa. It has been unexpectedly found that in defatting cocoa to obtain a substantially completely fat-free cocoa powder (>99% fat-free), such as by defatting with a supercritical fluid, e.g., CO₂, the resulting powder is rendered hypoallergenic, without the need for heat denaturation of protein allergens as described in U.S. Pat. No. 4,078,093.

At supercritical conditions, CO₂ exhibits the properties of both a gas and a liquid, and is thus used as a solvent, without leaving a toxic residue. CO₂ is preferred as the supercritical fluid since other defatting solvents, most notably hexane, may leave a residue which can cause an adverse reaction in allergic and asthmatic patients.

Without wishing to be bound by any theory, it is believed that removal of the fat from cocoa powder may impact on the three-dimensional structure of the protein component of cocoa, such that the human immune system will no longer recognize the proteins contained therein as allergens. Defatting also results in removal of mold, which may contribute to allergenicity.

The fat-free cocoa powder described herein may be distinguished from the heat-treated cocoa powder of U.S. Pat. No. 4,078,093. The latter contains substantial amounts of fat, at least 8%. The defatted hypoallergenic cocoa powder is used as a flavoring for the whey permeate.

The defatting process results in the elimination of mold, since the coating of microscopic mold spores comprises fat. Removal of yeast mold allows the cocoa powder to be utilized in soft drink plants, where the presence of mold is highly undesirable. Moreover, many patients allergic to chocolate are also allergic to other mold-containing foods, such as wine and cheese. It is believed that removal of the mold may contribute to the reduced allergenicity of the fat-free cocoa powder.

Essentially fat-free (>99% fat-free, more preferably at least 99.95% fat-free) cocoa powder may be prepared by defatting treatment of cocoa powder with supercritical CO₂. It may be prepared according to the process of U.S. Pat. No. 3,923,847. Cocoa powder is contacted with carbon dioxide which has been brought to supercritical conditions in respect to temperature and pressure. Pressures above 75.3 atmospheres, which is approximately equal to the CO₂ critical pressure, and temperatures above the CO₂ critical temperature (31.6° C.), are necessary for fat extraction. In practice, a pressure above 100 atmospheres gauge, and preferably between 200 and 400 atmospheres gauge, may be used. It is only necessary to work slightly above the critical temperature of CO₂. Preferably, the temperature is in the range of from about 40° C. to about 60° C. The contact time may generally comprise from about 2 to about 10 hours, with 4-5 hours being preferred.

The dairy permeate product may be stored in dry powder form and reconstituted with filtered water or soda as a sports exercise or electrolyte replacement beverage. Per unit of dry weight the product contains no fat, compared to 5.4% fat in skim milk and up to 38.3% fat in whole milk, based upon dry weight. In medical or veterinarian therapy one would strive for therapy greatly minimizing the risk or in most cases completely avoiding the risk of major or minor adverse side effects along with a high degree of therapeutic efficacy including anti-inflammatory, anti-rejection, synergistic activity, tissue healing capacity along with disease repair tissue proteins synthesis and re-synthesis, along with cumulative beneficial healed tissue effects highly competitive to corticosteroids in that relapse in major disease with stopping the medication does not occur for as long as six to twelve months or even longer as is the case with subject composition and its component optically active L amino acids and amino acid glycine (optically inactive neither L nor D).

This favorable efficacy coupled with dramatic tissue healing effect of therapeutic subject composition components L amino acids and amino acid glycine (optically inactive neither L nor D) analogue not only in structure and function to NSAID, 5ASA but also analogue and mimicking in structure and function to human tissue, specifically also analogue and mimicking the newest forefront of pharmacologic therapy, the human stem cell, (while not requiring human tissue). All of these beneficial functions and structures are dependent upon not only upon the 3D levorotary optical activity but also the left handed spin of electrons emitted from L amino acids and its 3-D tetrahedral spatial configuration and upon the alpha amino alpha carboxylic high-energy carbon and its contribution to the 3D tetrahedral spatial configuration, but also highly dependent upon L for amino acid. In this case also stimulating, activating and facilitating tissue healing and tissue protein synthesis and re-synthesis, and of molar ratios analogue to and mimicking human tissue. The subject therapeutic composition is thereby also an analogue to biochemical and immunologic sell and thereby minimizes potential adverse side effects.

In further contrast the aromatic benzene ring amines and its anti-inflammatory compounds derived from aniline, exhibit (#10) such as acetaminophen and its progenitors including aniline stack in a planar fashion of planar layers of benzene ring electron cloud compounds and further are not separated by a two carbon bridge containing the alpha carbon and its alpha amino alpha carboxylic acid key pivotal carbon to tissue healing protein synthesis grouping (exhibit #5 vs 5 ASA).

All of these beneficial functions and structures are dependent not only upon the 3-D levorotary optical activity but also upon the left handed spin of electrons emitted from amino acids and pivotally dependent upon the alpha amino alpha carboxylic high-energy ionizing side chain grouping carbon and its contribution to the 3-D tetrahedral spatial configuration which endow these L amino acids with their tissue healing protein synthesis capacity synergistically along with noncovalent bonding forces.

This can best be visualized and exemplified by exhibit (#10 a.) in contrast to exhibit (# 10) comparing structurally for example the three carbon organic acid propionic acid anti-inflammatory derivatives such as but not limited to naproxen and ibuprofen wherein the potential alpha carbon next to carboxylic add group, exhibit (#3) and (U 3a.) fails to contain the amino group characteristic of the tissue healing features of the L amino acids in addition to its anti-inflammatory side chains positioned on its second carbon as is the case for example of L alanine or the aromatic amino acids such as but not limited to tyrosine, tryptophan or phenylalanine.

Bonding and Special Bonding Techniques to Incorporate L Amino Acids

(1) utilizing the analogues including reactive side chain groups with corresponding to medicaments as analogue corresponding therapeutic agents of L amino acids.

Such as, but not limited to the acetylation of the phenolic hydroxyol groups of tyrosine or serine, as an ester, by esterification or utilization ethyl alcohol as a reactant molecule with these hydroxyl groups forming ethers by etherification including chemical bonding with such component amino acids as serine, tyrosine, hydroxy glutamic acids. The resultant antiinflammatory activity is analog to aspirin, acetyl salicylic acid, in structure and function of the acetyl group in that this grouping can inactivate the end serine grouping of the inflammatory prostaglandins synthesizing enzyme, prostaglandins synthetase. This action is lost in the non-acetylated salicyclic acid.

(2) These reactive moieties side chain groupings and ionizable and very high-energy groupings may be utilized in an analogue therapeutic format and such as but not limited to groupings include guanidinium group of arginine, the beta carboxyl group aspartic acid, the thiol group of cysteine and the gamma carboxyl group of glutamic acid and the imidazole of histidine, the episolon amino group of lysine, the reactive phenyl group of phenylalanine and the reactive pyrrolidine of proline.

The high-energy alpha carboxyl groups and alpha amino groups of all the amino acids may all be used as reactive chemical; linkages to the other two components of this stem cell composition.

Phospholipids as P.C. or lyso lecithin with its available hydroxyl group and/or extracellular matrix components, such as, but not limited to, collagen or procollagen tropocollagen and its available hydroxyl groups as in hydroxyproline and hydroxylysine. These include all available chemical bonding techniques including condensation.

The hydroxylated fatty acids of ricinoleic and hydroxy stearate including but not limited to cyclic amino acids and cyclic fatty acids are also available such as but not limited to chalmougric and hydnocarpic fatty acids hybridizing by bonding to phospholipid lysolecithin such as ester or ether bonds. Also doable with the cyclic and/or hydroxylated amino acids.

The concept of treating plaque in a prevention at or active stage involves addressing the plaque as not being part and parcel of the metabolic metabolizable internal milieu or soluble internal milieu or a variant, of hydrophilic/lipophilic or more broadly expressed as hydrophilic/hydrophobic balance to permit rheologic flow and homeostatic internal milieu balance, immunologic-self internal milieu as is exemplified by subject composition and its components and reversing same by foregoing bonding technology as applied to subject composition and its components. These plaques may be best exemplified by atherosclerosis, Alzheimer's disease, inflammatory diseases, resistant chemoattractants in inflammatory disease, aging associated with progressive deficiency in phospholipid surfactant for example but not limited to phosphatidyl choline.

The universal donor essence of stem cell subject composition, when given orally may also be therapeutically and simultaneously stimulating oral tolerance to prevent and reverse progressive immuno-inflammatory organ damage reactions. These reactions further aggravate organ damage to such degree that the organ beings to deviate from self as in congenital biliary atresia. That in turn may already be mounting a rejection reaction. These are the steps that subject composition are preventing in averting the need for organ transplant. Should a transplant still be required, with oral tolerance so established and with the continuation of subject composition and its beneficial therapeutic effects will decrease the rejection mechanism, thereby decreasing the need for very high risk, life-time requirement of the anti-rejection armamentarium of medications.

In the prevention of rejection which occurs even in the most carefully HLA matched donor transplant, we find that even though the patient is normally replacing and re-replacing tissue and organ systems in an orderly progressive fashion every 2 to 3 months, the spark of rejection has been ignited and initiated and continues indefinitely even with this repeated spontaneous replacement with patient's own tissue and organ system. This knowledge emphasizes the importance of constantly preventing the rejection immune inflammatory conflagration from being initiated, as is being done with subject composition, as in congenital biliary atresia, working in concert with the gastrointestinal tract's oral tolerance, digestive enzymatic metabolic processing and solubilization, and HLB PC modulation by liver, gall bladder, biliary system.

Emphasizing the advantage in subject composition that are component analogue match of the diseased tissue and organ (such as but not limited to heart, lung and bronchopulmonary tract, and kidney urinary tract, liver, spleen, bone marrow, undergoing treatment). The criteria of components of subject composition also include being amenable to the body's metabolic processes, being readily solubilized in the internal milileu along with HLB modulation to practicalize solubility and extracellular matrix, cell membrane and/or intracellular delivery as required.

The neurologic degenerative diseases associated with aggregate proteins include, but are not limited to prion diseases—transmissible spongiform encephalitis derived from mad cow and allied diseases (aggregate/inclusions, of abnormal protein prion beta pleated sheet (PrPsc) non-metabolizable, resistant to the enzymatic activity of proteinase K. Abnormal protein deposits are seen histopathologically, instead of the normal alpha helix isoform (Pr Pc) normal brain proteins structure extracellular and not aggregate/non-inclusion and random coil normal structure extracellular brain protein. Alzheimer's has similar inclusion/aggregate beta pleated sheet, amyloid instead of the normal alpha helix and random coil normal structure and non-inclusion/non-aggregate extracellular brain protein. Insoluble nuclear brain protein aggregates are found in Huntington disease (the abnormal protein being Huntingtin protein) and spinocerebellar ataxia and (Ataxin) instead of the normal structure of trinucleotide repeats.

Parkinson's disease also has an abnormal protein alpha synuculein intracytoplasmic aggregate/inclusion. Lewy bodies instead of normal random coil repeat proteins structures, cancer with deficiency in HLB modulation and adequate surfactant required by DNA progress through normal rheologic flow required in mitosis with normal cellular and nuclear division and sharing of DNA genetic traits and the resultant formation of normal daughter cells. The darkly stained nuclear mitotic figures makes its appearance as an aggregate plaque or precipitate removed from the normal flow of nuclear function and the microcirculation of nuclear DNA genetic nuclear focus and originating cell division. Response to hydrophilic surfactant in vitro is supportive of this thesis (83 percent of the breast cancer cells were killed in 24 to 48 hours with exposure to 0.25 percent polysorbate 80, Tween 80). Again countering the poor solubility of the plaque-like mechanism disease which contributes to metabolization and the normal metabolic turnover of all cell tissue and organs brings about a disease-free therapeutic response. About one-third of these cancers are associated with inflammatory immunologic response T lymphocytic-plasma cell changes and are of poor prognosis. Response to HLB modulation towards a hydrophilic HLB has provided an 83 percent in-vitro encouraging response reported in other embodiment.

Another poorly metabolizable plaque producing substances of atherosclerosis are the trans fatty acids fats. These fats whose melting points are now significantly above body temperature and may be as high as 150 degrees Fahrenheit functioning as solid insoluble fats even though they may be as much as 20 percent unsaturated. For these two reasons they are not available to the internal milieu to be processed as self are a soluble metabolic team player, and therefore processed as foreign or foreign body likened with resultant plaque formation and atheromatous change and associated inflammatory changes.

With similar plaque disease mechanisms of insolubility, or insolubility aggregates, non-metabolizable, and immunologically foreign or nonself therefore maybe additionally be inclusive of pneumoconiosis such as but not limited to asbestosis (asbestos being a product of volcanic ash and igneous rock with a 5 fold increase in lung cancer with exposure to another product of combustion), tobacco smoke (an adverse synergistic catalyst, in a sense synergistically and pathologically additive as two products of combustion), exposure and now there is a 55 fold increase in lung cancer, silicosis and coal workers disease. This may be exemplified than not limited to asbestos, a volcanic ash fiber of silica calcium and magnesium therefore a product of a thoroughly burned rock derived product and not available for metabolic combustion, its insolubility has been estimated and extrapolated to be cells insoluble that is finally solubilized in more than 400 years of contact with water therefore foreign to tissue and immunologically non-self. Another insoluble crystal disease includes the insoluble uric acid crystals of gout (even though theoretically metabolizable).

Again, HLB modulation by enhancing hydrophilic solubility and more favorable hydrophilic/hydrophobic ratios should prove therapeutically useful. The use of PG PR to emulsify and disburse the fat and provide a lubricant for these physically abrasive sandpaper like crystals prior to hydrophilic solubilization.

These foregoing methodologies may be looked upon as basic principles of application technology and considerations in developing present and future pharmaceutical products. The fact that uric acid crystals are very soluble in glycerine, in contrast to marked insolubility in water and therefore in the fluids of tissue, may be used in therapy of gout starting with ½ to 1 teaspoon glycerine 3 to 4 times daily followed by a glass of water.

This anti-inflammatory activity in association with tissue healing activity of the L amino acids in subject composition Q1 01 KC was successfully utilized in congenital biliary atresia (CBA) preoperatively in averting and saving the reported infant from a liver transplantation was reported along with the successful management of Crohn's disease in Girsh's patent applications and scientific exhibits presentations (exhibit 19). This antirejection pharmacodynamic activity is companion to and synergistic to the anti-inflammatory activity of the L amino acids analog and molar ratios to the cyclic oligopeptides amino acids of cyclosporine and include the following L lysine, L alanine, L valine and glycine.

Also successful in anti-inflammatory tissue healing as well as anti-rejection activities reported in postoperative use in 11 patients by the Johns Hopkins pediatric surgery group as Q1 01 KC and as a similar source for subject composition L amino acids, alimentum. In CBA the patient's liver is so damaged by inflammatory disease and the integrity of immunologic self must be significantly modified and so may be looked upon by the body immunologically as foreign and significant rejection reaction must be a factor that was also reversed in the severe inflammatory response, yet associated with remarkable anti-inflammatory tissue healing activity of L amino acids of Q1 01 KC. This associated antirejection activity must also have been present to reverse immunologic hypersensitivity states suspected not responsive to the very potent antirejection therapy being used in the 11 postoperative post transplantation Johns Hopkins pediatric surgical group CBA patients.

This union of biochemical essence in synergy and cosynergy into and/of biologic structures companion to their function and multiplicity of functions applied to anti-inflammatory activity and healing is as unique and analog and structured function as the government United States of America and progressive union of structure from borough to township to city to state to federal government as well as synergistic function and multiplicity of functions and is highly unique in contrast to what is available with those skilled in the art(s). These biochemical essence of subject composition are not only analog to these organizational systems as well as analog to therapeutic medications reactive high-energy side groupings as well as ionic groupings of stem cell result in and continue in perpetuation to the production of cell and the embryonic stem forming extracellular matrix tissue, organ systems, and vital organs are all under cooperative control of the central and peripheral nervous system autonomic nervous system, immunologic systems, nervous system like memory, and neural hormonal systems.

While not wishing to be bound to any theory, this tetrahedral 3-D spatial conformation is also evident not only in the L amino confirmation and glycine but also in these two carbon molecular two carbon bridges which also separate and keep the aromatic amino acids in this 3D tetrahedral formations. A distinctive from the planar benzene ring 3-D conformation that stack and slide one upon the other subject composition and its components are also analogue to and mimic the noncovalent bonding technology resulting in the elaborate cellular architecture visible in the electron micrographs of mammalian and human tissue and human stem cell tissue mimicking in being analogue to the most important noncovalent chemical bonding of human tissue and human stem cell tissue.

It is interesting and highly applicable to note that the phosphate molecule so pervasive in all metabolic activities is also tetrahedral in 3-D shape and could very well represent the reason for glucose and fructose phosphorylation as glucose six phosphate, fructose six phosphate, fructose 1 6 phosphate as a structural bioengineering fit and therefore functional fit in the utilization of glucose in energy production and release to the body suggesting advantages to these analogue 3-D tetrahedral spatial fit in the therapy of diseases such as but not limited to diabetes mellitus.

Subject composition and its component L. amino acids and glycine is analogue and mimics not only in structure and function anti-inflammatory drugs such as but not limited to NSAID, 5ASA, (Exhibit #5, 5a, 10, 3), as well as being analogue and mimicking anti-rejection medication such a cyclosporin, but also is analogue and mimics in structure and function human tissue, specifically also analogue and mimics the newest forefront of pharmacologic therapy, the human stem cell, (while not requiring human tissue, requiring only its biochemical equivalent essence as illustrated in prior embodiments). In this case also stimulating, activating and facilitating tissue healing and tissue protein synthesis and re-synthesis, and of molar ratios analogue to and mimicking human tissue. The subject therapeutic composition is thereby also analogue to biochemical and immunologic self and thereby minimizes potential adverse side effects.

The bioengineering therapy at a molecular level therefore requires providing this stereochemical 3D fit of L amino acids and glycine therapeutic subject composition. This stereo biochemical fit into the DNA, ribosome, transcription of tissue healing also maximizes the therapeutic fit and therefore therapeutic activity of the L amino acids and glycine reactive high energy ionizing side chain that stimulates the simultaneous overlap and continuum as conjoint therapeutic activity, exemplified but not limited to, anti-inflammatory tissue repair protein synthesis activity. These 3D conjoint therapeutic activities are further synergistically enhanced by HLB modulation to insure the best biomolecular therapeutic targeted fit required for cell membrane and for cell delivery system and/or extracellular matrix delivery synergistically adaptable to disease in question as the newest stem cell therapy.

To best synergize these therapeutic healing activities with current and future medications while simultaneously fulfilling these bio-molecular tissue 3D fit needs, the following requirements must be fulfilled: (a) by using the foregoing stereo biochemical L or Levo optical rotation of light and energy and alpha amino, alpha carboxylic side chain ionizing groups, as free L amino acids and glycine's structural back bone with their therapeutic ionizing high energy side chains with additional synergy by adding further therapeutic side chains and therapeutic moieties such as, but not limited to, the acetyl radical or the indole radical, (b) by adding current or future medications to bond biochemically by hydrogen bonding, van der Waals forces electrostatic and zwitterion forces. (c) by covalent or valent chemical bonding or bridging of current or future medications to items as described in subject composition in (b), and (d) by biochemical and bioengineering bonding the biochemical therapeutic moieties to (a and/or b and/or c).

In the bioengineering design of a medication to be analogue to human tissue and to human stem cell, (the most advanced forefront of pharmaceutical therapy), the most common and most abundant bonding forces of human tissue is the non-covalent bonding force of human tissue and therefore of subject composition analogue to and mimicking human tissue and stem cell and biochemical essence of stem cell. It is not taught in the prior art that subject composition biochemical components, extracts and essence of non human tissue and non human tissue stem cells can non-covalently bond and result in human tissue signaling systems analogue to human stem cells resulting in a combination of several therapeutic effects including but not limited to anti-inflammatory effects, overlay and continuum of disease tissue healing effects, and tissue protein synthesis in re-synthesis in healing diseased tissue.

It is this flexible access to healing that makes non-covalent bonding so important in tissue healing and tissue protein synthesis and re-synthesis, it is this very weakness (10 to 100 times weaker in kilojoules per mole) of these non-covalent bonds that allows them to be repeatedly and continually broken and repeatedly and continually reformed in the dynamic interplay that is life, health, and tissue healing.

This continual and repeated interplay depends on rapid interchange of molecular partners which could not occur if intermolecular bond forces as in the case of valent and covalent bonding are so fixed and rigid as to lock the molecules up in a rigid inflexible intermolecular conformation to obstruct a very flexible availability as in subject composition so important in a therapeutic medication as in these subject composition embodiments in tissue healing, protein synthesis and resynthesis healing offered so unique to this subject composition, the use of non-covalent bonding (Covalent bonds of 300 to 400 kilojoules per mole are exemplified by but not limited to carbon-carbon bonding and carbon-hydrogen bonding and present in the aromatic and aliphatic carbon chains of L amino acids and glycine of subject composition).

Covalent bonding is similar to bonding currently available in synthesized medications. Further examples of noncovalent bonding application technology of subject composition in molecular bio engineering in tissue healing and cell, tissue and organ reconstruction and reconstructive repair of cellular, tissue and organ disease. The efforts dedicated to the health-care and pharmaceutical industry mission to utilize, such subject composition in healing of disease and reversal to normal of cellular, tissue and organ disease along with protein synthesis and resynthesis in diseased tissue repair utilizing subject composition in noncovalent bonding associated with (1.) DNA (2.) the protein molecule (3.) the macro molecular protein superstructure of the cell, tissue and organ in heeling. The therapeutic application such as but not limited to the noncovalent bonds as presented therapeutically in subject composition available in subject compos Won to stabilize:

(1.) DNA's interaction between different parts of the strands of the structural and functional DNA macromolecule composed of linear sequenced (and covalently bonded) nucleotide residues.

(2.) Proteins all made up of covalently bonded amino acids (similar in many respects, and being in actuality a transcriptive reflection of the DNA and RNA template of the macro molecule DNA) are folded into specific 3 D molecular informational as well as conformational arrangements by non covalent bonding energy forces as available in subject composition and utilized in many embodiments presented for tissue healing and tissue proteins synthesis and resynthesis.

The many noncovalent interactions provided by subject composition which stimulated, facilitated, accelerated, activated and synergized by subject compositions noncovalent bonding activity in an analogue and mimicking fashion to human tissue and human stem cell tissue and the biochemical essence of stem cell as utilized in subject composition.

(3.) Subject composition stimulates facilitates accelerated activates proteins interaction with other protein molecules or with other macromolecules such as DNA to form even higher levels of organization leading to the healing of cell, tissue, and organ of diseased cells, tissue and organs there such as but not limited to the application of subject compositions biotechnology to inflammation provides healing formation tissue healing protein synthesis and resynthesis in healing and reformation of a disease.

While not wishing to be bound to any theory this noncovalent bonding support by subject therapeutic composition of macromolecules such as but not limited to foregoing embodiments (1.), (2.), and (3.) DNA, RNA and resulting transcription protein appears to be a form of noninvasive DNA bio-engineering with minimum if any risk factor in patients such as but not limited to Crohn's disease and pediatric Crohn's disease where hereditary factors are suspected in playing a significant role

(e.) However, microorganism, (such as but not limited to fungal) derived medications may contain the D amino acid components such as but not limited to cyclosporine, designed for humans and animals, however may not be metabolizable with the presence of L amino acid enzymes and the absence of D amino acid enzymes in humans and animals. These D amino acid components are not readily metabolizable therefore a factor in recognition of biochemical and immunologic self and therefore predisposing to adverse side effects.

This risk factor may be exemplified by the anti-rejection therapeutic agent oligopeptide cyclosporine with the multiplicity of major side effects including the 20 percent risk of loss of renal function contain the D alanine amino acid, which is also found in microorganism (bacterial) cell wall along with D glutamate components of microorganism polypeptides

Therefore, resynthesis of such valuable drugs as cyclosporine would be value with subject composition components as illustrated but not limited to subject composition generic code Q101KC, by substituting L alanine for microorganism derived D alanine would make this drug more compatible in bioengineering to biomolecular self and to immunologic self identity thereby greatly reducing the risk, major adverse reactions such as 20 percent loss in renal function. This advantage is also offered by subject composition with its L amino acids and glycine in molar ratio with cyclosporine such as glycine, L alanine, L valine, L leucine and gamma amino butyric acid along with methyl donors such as, but not limited to, methionine and betaine, with its ability to function as an anti-rejection pharmaceutical activity in vivo. This subject composition analogue mimicking of such structure and function as cyclosporine may come about by the in vivo resynthesis of cyclosporine with L alanine instead of D alanine or by synthesis stimulation facilitation or acceleration of the pharmacologic effects of and metabolite effects of cyclosporine and or by using methodology of and including non covalent bonding of subject composition such as but not limited to embodiments of application technology.

These methodologies will provide therapeutically efficacious, minimum risk drugs for diseases such as but not limited to pediatric Crohn's disease or congenital biliary atresia and their major complicating subsets, that is the same drug as patent pending subject composition.

Subject composition generic code Q101KC contains components, optionally in molar ratios similar to, that provide for specific application as anti-inflammatory therapeutic agents comprising free L amino acids and the optically inactive (non D non L) amino acid glycine, and specified molar ratios analogue and mimicking human tissue, that is both analogue to and mimicking NSAID (including Vioxx and Celebrex, the newest NSAID) and synthetic amino acid 5ASA and NSAID anti-inflammatory drug, anti-rejection medication (more specific to 5ASA in being analogue and mimicking anti-rejection drug cyclosporine), while at the same time as well as being analogue and mimicking human tissue and human stem cell tissue and stimulating, activating and facilitating tissue healing, disease repair, and tissue protein synthesis and resynthesis,

L amino acids and amino acid glycine (optically inactive neither L nor D) analogue not only in structure and function to NSAID, 5ASA but also analogue and mimicking in structure and function human tissue. Specifically the subject composition is also analogue to, and mimics, the newest agent at the forefront of pharmacologic therapy, the human stem cell, (while not requiring human tissue), in this case also stimulating, activating and facilitating tissue healing and tissue protein synthesis and resynthesis, and of molar ratios analogue to and mimicking human tissue. Q101KC therapeutic composition is thereby also analogue to biochemical and immunologic self and thereby minimizes potential adverse side effects. The L amino acids and glycine amino acid, including both aromatic and aliphatic amino acids of Q101KC, clearly delineated and well documented by controlled studies regarding efficacy and scientific rationale as presented. The aromatic amino acids of Q101KC are analogue and mimic medication in function and structure of the aromatic amine synergism of triple sulfonamides as well as the other L amino acids and glycine.

In this specific application for drug designation the amino acids should be available entirely as therapeutically active free L amino acids and non L or D glycine amino acid and, therefore, should be free of such residual polymers as hydrolyzed protein source peptides.

To recapitulate such therapeutic activities such as but not limited to: not only anti-inflammatory (such as but not limited to NSAID, 5ASA) anti-rejection (such as but not limited to cyclosporine), synergistic activity but uniquely also, analogue to and mimicking tissue healing, tissue proteins synthesis, tissue protein resynthesis. Added advantages and highly competitive to the corticosteroids include cumulative beneficial healed tissue effect, the lack of relapse with stopping this medication for as long as six months, one year, even longer, exhibits #1 through #20. As set forth in Exhibits 1-21, PCD denotes Crohn's disease; CBA denotes congenital biliary atresia; and Q101KC is a designation for the compositions of the subject application (e.g., NEOCATE or VIVONEX).

Such a therapeutic result is possible in view of the biochemical and pharmacologic structure and function of a component for example but not limited to the L amino acids and optically inactive (non D and non L) amino acid glycine offering medical and veterinary practice a competitive edge over microorganisms of very primitive background and origin. However, microorganism, (fungal) derived medications may contain the D amino acid components designed for humans and animals with the presence of L amino acid enzymes and the absence of D amino acid enzymes in humans and animals, these components are not readily metabolizable therefore a factor in recognition of biochemical and immunologic self and therefore predisposing to adverse side effects.

This risk factor may be exemplified by the anti-rejection therapeutic agent oligopeptide cyclosporine with the multiplicity of major side effects including the 20 Percent risk of loss of renal function contain the D alanine amino acid, which is also found in microorganism (bacterial) cell wail along with D glutamate components of microorganism polypeptides.

Further incorporated in this structure exemplified by, but not limited to, the aromatic amine t. amino acids and non D non L glycine: is that the high energy benzene ring is always separated from the amine or amino high energy group by a 2 carbon ethyl grouping (bridge like biochemical separator) whereas the aniline dye, coal tar potentially toxic and benzene ring derived biochemical compounds exhibit 10 are directly attached to the benzene ring with other groupings attached in the ortho, meta, or para positions are dissimilar to biochemical and/or immunologic identity as self and as expected have a high incidence of adverse side effects. These adverse side effects can be minimized or avoided by using the aromatic amines or other benzene ring derivative medications with subject composition as a protective shield, or by deriving such medicines such as but not limited to anti-inflammatory 5ASA a synthetic amino acid NSAID, and the newest anti-inflammatory medications such as but not limited to Vioxx and Celebrex from the synthetic L amino acids and non L non D glycine amino acid. This may be accomplished by biochemical bonding reactions such as, but not limited to acetylation or hydroxylation first followed by acetylation. in addition to etherification, condensation, condensation and amination chemical reactions may be applied to obtain these safer derivatives.

To recapitulate: in medical or veterinarian therapy one would strive for therapy greatly minimizing the risk or in most cases completely avoiding the risk of major or minor adverse side effects. was such therapeutic activities such as but not limited to: not only anti-inflammatory (such as but not limited to NSAID, 5 ASA) anti-rejection (such as but not limited to cyclosporine), synergistic activity but uniquely also, analogue to and mimicking tissue healing, tissue, proteins synthesis, tissue proteins on resynthesis.

Added advantages and highly competitive to the corticosteroids include cumulative beneficial healed tissue effect, the lack of relapse with stopping this medication for as long as six months, one year, even longer (exhibits #1 through #20). Such a therapeutic result is possible in view of the biochemical and pharmacologic structure and function of a component for example but not limited to, the L amino acids and non D and non L amino acid glycine over microorganisms of very primitive background and origin. For example microorganism, (fungal) derived oligopeptide cyclosporine with the multiplicity of major side effects including the 20 percent risk of loss of renal function, D glutamic acid, D alanine both microorganism and (bacterial) cell wall components of polypeptide.

Further incorporated in this structure exemplified by, but not limited to, the aromatic amine L amino acids and non D non L glycine: is that the high energy benzene ring which is always separated from the amine or amino high energy group by a 2 carbon ethyl grouping (bridge like biochemical separator); whereas the aniline dye, coal tar potentially toxic and benzene ring derived biochemical compounds are directly attached to the benzene ring with other groupings attached in the ortho, meta, or para positions are dissimilar to biochemical and/or immunologic identity as self and as expected have a high incidence of adverse side effects.

These adverse side effects can be minimized or avoided along with adding tissue healing effects not already present by using the aromatic amines or other benzene ring derivative medications along with subject composition as a protective shield, or by deriving such medicines such as but not limited to anti-inflammatory 5 ASA a synthetic amino acid NSAID, and the newest anti-inflammatory medications such as but not limited to Vioxx and Celebrex from the synthetic L amino acids and non L non D glycine amino acid (above methodology of a to e).

This may also be accomplished by bonding L amino acids to these existing NSAID or 5ASA Vioxx Celebrex by acetylation or hydroxylation first followed by acetylation. in addition to esterification, etherification, condensation amination and/or transamination chemical reactions may be applied to obtain these safer derivatives. Additionally further pharmaceutical advantageous therapeutic functional properties may be added to L amino acids and glycine may be added by bonding pharmaceutical active moieties by such chemical bonding methods including but not limited to the foregoing. On further analysis these biochemical structures and associated functions serve as a basis for this unique pharmacologic function of healing and the stimulation, facilitation, acceleration of healing.

These structures are based on the biomolecular analogue mimicking and therefore biochemical and immunologic identifying features of self as a basis for minimizing adverse reactions are also present This has not been taught in the prior art By aminating the alpha carbon (that is the second carbon next to the carboxylic acid) the organic acid derivatives that also has the anti-inflammatory (for example but not limited to naproxen or ibuprofen or other anti-inflammatory propionic acid derivatives, anti-inflammatory butyric acid derivatives, anti-inflammatory caproic acid or other 2, 3, 4, 5 organic acid anti-inflammatory derivatives) biomolecular properties (or other outstanding pharmacologic properties) the biomolecular tissue heating tissue protein synthesis and resynthesis therapeutic properties are now hereby added to the therapeutic activity of the medicament

This is particularly reinforced as the molecule is in the 3D L chiral (optical levorotary form) and already existent if the base starting molecule is already an existing L amino acid. Whereas, if the base starting molecule is a 2, 3, 4, 5 or 6 carbon organic acid it is preferable that the chemical process of alpha carbon amination is so provided to include only the L chiral (optically levorotary form). Thereby using these principles of biomolecular engineering the opportunity is being offered here to add tissue healing qualities to any medication or potential medication in addition to reducing the risk of adverse side effects including maintaining a biochemical self as well as an immunologic self identity as well as a very valuable cumulative effect even after the medication is stopped, therefore highly advantageous and competitive over corticosteroids.

While not wishing to be bound to any theory the tendency of the benzene ring and its therapeutic derivatives to stack and not be involved in the tissue healing thread associated with tissue proteins synthesis and resynthesis may help to explain the fundamental differences in the lack of tissue healing efficacy and adverse side effects versus 3-D L amino acids and glycine. This chiral asymmetry of the L. amino acids in the subnuclear electron behavioral activity, gives electrons emitted (in beta decay) a left-handed spin in free L amino acids and glycine therapeutically. Therapeutically also gives higher form of life such as but not limited to humans a strategic advantage and often critical competitive advantage over primitive microorganisms for example in the biomolecular homeostatic internal milieu of health vs. disease.

Therefore, resynthesis of such valuable drugs as cyclosporine with L alanine substituting for D alanine would make this drug more compatible in bioengineering to biomolecular self and to immunologic self identity thereby greatly reducing the risk, major adverse reactions such as 20 percent loss in renal function. This advantage is also offered by subject composition with its L amino acids and glycine in molar ratio with cyclosporine such as glycine, L alanine, L valine, L leucine and to L gamma amino butyric acid with its ability to function as an anti-rejection pharmaceutical activity in vivo. This subject composition analogue mimicking of such structure and function as cyclosporine may come about by the in vivo resynthesis of cyclosporine with L alanine instead of D alanine or by synthesis stimulation facilitation or acceleration of the pharmacologic effects of and metabolite effects of cyclosporine.

Again, while not wishing to be bound to any theory, the tendency of the benzene ring and its therapeutic derivatives to stack and not be involved in the tissue healing thread associated with tissue proteins, synthesis and resynthesis, necessary for recovery, may help to explain the fundamental differences in the lack of tissue healing efficacy and adverse side effects in contrast to the above-mentioned 3D effects of the L amino acids. (in contrast these stacked planar benzene ring molecules function as electron clouds whose fluctuating force cause the planar molecules to slide, without touching, one upon the other)

This 3-D effects can be even further synergized by advantageous HLB modulation for example HLB of 18 to 20 respectively, 0.25 percent to 0.5 percent such as Tween 80 or sodium lauryl sulfate in the face of severe infection, locally or systemically and poorly responsive or completely unresponsive to antibiotic (which can be documented further, in each case, by comparative bacteriologic studies) including antibiotic sensitivity and staining characteristics before and after HLB modulation can be used to inactivate lipids, lipoproteins, such as, but not limited to, lipid A (glycolipid endotoxic activity) and weaken the microorganisms (such as but not limited to bacteria, viruses, and/or fungal pathogens and their products) cell wail offensive microorganisms such as but not limited to therapeutically challenging microorganisms such as but not limited to E. coli, Pseudomonas aeruginosa, anthrax and its spores—or protein lipopolysaccharide tuberculin cell wall tuberculin of mycobacterium tuberculosis, (or resistant mycobacterium tuberculosis and its lipopolysaccharide cell wall, as occurs for example in HIV infections). Viral infections including HIV efficacy results from the respective enhancement of so-treated (IHLB modulation) antibiotics which can by HLB modulation, be made more been penetrable and efficacious.

This treatment can be preceded by the HLB of 2, 0.25 percent to 1 percent, PGPR (polyglyceryl polyricinolate) as an aid in disbursing the microorganism's cell wall fat and make it more available to foregoing high HLB therapy. In other embodiments this has also been shown to reduce the pathogenicity and specificity of the allergenic pathogens.

Successful anticancer therapeutic activity cancer tissue cell in vitro, breast cancer cell suspension comparative trials with treatment with 0.25 percent to 0.5 percent polysorbate 80 (Mean 80) with 83 percent reduction in 24 to 48 hours of cancer cell mitochondrial activity after HLB modulation with tween 80, and 50 percent reduction in cancer cells' abnormal morphology and abnormal mitosis on cytopathologic review. This high HLB therapy of 18 with, Tween 80 could have been mediated and had an antiviral effect on potential oncogenes, or countered a lipophilic carcinogen by reducing its lipophilic pathogenicity or could have permitted a more normal flow of nuclear chromosomal fluidity (prior embodiments have shown mitotic figures in the nucleus to appear as plaque like precipitates, with interference with normal rheologic nuclear cell division flow) much higher hydrophilicity is required in more normalized cell division in mitosis by adding deficient hydrophilic surfactant required for normal mitosis.

Not taught in the prior art:

Current therapeutic agents such as but not limited to the anti-inflammatory agents lack a tissue healing component. This is in sharp contrast to the anti-inflammatory therapeutic L amino acid glycine components of subject composition which have a dual action ant-inflammatory and tissue healing bonded bridge. The primary pharmaceutical molecular differences are illustrated here in exhibits 3 and 10.

1. There is a two carbon ethyl bridge separating the aromatic amino acid high-energy benzene ring from its amino side chain group (Exhibit 3) whereas in exhibit 10 the anti-inflammatory acetaminophen compound derived from aniline (and historically the aniline dye industry and coal tar industry), and other pharmaceutical derivatives such as but not limited to those shown here are lacking in this ethyl two carbon breech separating the amino group from the high-energy benzene ring anti-inflammatory aromatic amine compounds so bonded with a 2 carbon ethyl bridge should enhance the tissue healing efficacy of these compounds (not only not present but actually without this two carbon ethyl there is not only an absence of tissue healing effect but actually an inhibition of tissue healing effect.

2. In exhibit 3 in the case of the propionic acid anti-inflammatory derivatives there is no amino group on the second (or Alpha) carbon for example ibuprofen or naproxen, and as there is in the eight propionic acid derivatives anti-inflammatory function L amino acids of subject composition have coexistent amino groups on the second or Alpha carbon imparting to these compounds the tissue healing pharmaceutical function.

In bioengineering future pharmaceutical compounds such as, but not limited to, anti-inflammatory propionic acid derivatives and amino group could be bonded to this site endowing these compounds with the additional tissue healing pharmaceutical function of subject composition (not only not present in current anti-inflammatory propionic acid derivatives but these current pharmaceutical compounds have an inhibitory effect on tissue healing).

This continuum of the inflammatory disruptive and destructive conflagration of disease proceeding to healing resolution (also an overlay of healing resolution) may be mediated by free L amino acids of the subject composition (herein referred to as Q1 01 KC). This destructive inflammatory process is expressed by the protease enzymes secreted by the neutrophile. This conflagrative inflammation of PCD (pediatric Crohn's disease) was originally triggered by a chemo-attractant response to injury and disease, foreign and non-self immunologically, and has demonstrated by in vitro preclinical and in vivo controlled clinical studies in a total of more than 250 patients has demonstrated the efficacy of free L amino acid subject composition turnoff signaling switch of free L amino acids in subject composition Q1 01 KC. And in the present application 5 to 15 grams dry weight (15.5 percent free L amino acids and glycine, or 775 mg, and analogue in 800 mg dosage of synthetic amino acid 5 amino salicyclic acid, to 2, 325 mg free L amino acids) in addition to free L amino acid produced by neutrophile enzymatic action in toto the therapeutic subject composition resulting stockpile of free L amino acids which in turn provides a simultaneous positive protein synthesis stimulus of replacement of damaged tissue under DNA guidance by the endoplasmic reticulum resynthesis of tissue protein associated with healing resolution. The PCD and CBA patients may now be grateful for the effective non-steroidal therapy now available with documented steroid-sparing actions.

With stimulus switch-off signaling mechanism the newly released neutrophiles are stimulated to leave the bone marrow to enter the inflammatory PCD site tracked by permeability test (exhibits 2, 1, and 12), simultaneously with the need for response to tissue injury stimulus turned off, the existing neutrophiles will migrate back to the reticulo endothelial system sites as seen in the permeability studies (liver and spleen).

Simultaneously again, with the autolytic enzymatic digestive response of the neutrophile silenced, the tissue healing resolution to former integrity is initiated, again with the stimulus of the added dosages of L amino acid, Q10 01 KC by way of the law of mass action promoting stimulus for resynthesis of tissue protein.

In addition to including free L amino acids analogue to and in molar concentrations of tissue as the biochemical essence of protoplasm in the embryonic stem cell subject composition, two other analogue categories of components, are included, which are also recognized as self and include the biochemical essence of cell membrane phospholipid such as but not limited to phosphatidyl choline, and extracellular matrix including, but not limited to, the first biochemical substance embryonic stem cells produce the extracellular matrix including but not limited to collagen (these components of subject composition are available as currently marketed products available for healing resolution of disease). The phospholipids such as phosphatidyl choline self vesiculates and provides cell membrane restoration as the biochemical essence of cell membrane in PCD and CBA.

This self vesiculating membrane restoration is synergistically aided in cell membrane repair, furthered by the free L amino acids of Q1 01 KC subject composition particularly glycine. Collagen, the extracellular matrix and the first biochemical substance embryonic stem cells produce, contains and is enmeshed and entwined in growth factors, and also offers, intrinsic to its structure, analogue computer software all tissue such as human tissue structure and function. Compositely as embryonic stem cell therapeutic composition and as individual components, these components are well-tolerated components and are looked upon by the body immunologically as self. (Whereas other therapeutic agents in their pharmacodynamics and pharmacokinetics are not bioengineered as analogue to human tissue and are therefore not recognized as self and may in the future be significantly enhanced with the use of this paradigm of pharmacodynamic and pharmacokinetic analogue of bioengineering design and therapeutic cell functioning design.) In fact if they have not been specially bioengineered for the inflammatory immune response overlay and continuum of healing resolution cycle, they may be looked upon or interpreted as foreign by the body's response to injury system. For example but not limited to NSAID such as indomethacin or aspirin wherein protein synthesis is inhibited and in the case of indomethacin neutrophile motility is also inhibited, this, of course includes protein required for healing preventing the normal retreat of neutrophile anti-inflammatory turn off signal. The antiinflammatory corticosteroids are well recognized for their interference with the healing cycle. Therapeutic agents which are not bioengineered to complete the therapeutics of the healing resolution process of inflammation, and are viewed by the body's immune inflammatory response system as foreign and their pharmacodynamic substance and metabolites represent the body's response to an injury and therefore, as we might expect, adverse reactions are also listed as possible occurrences.

The Q10 01 KC subject composition stem cell as a delivery system analogue to immunologic concept-self.

In contrast, this newly created subject therapeutic composition biochemical stem cell is representative of self and may serve as a delivery system for other therapeutic agents to be fit in and be looked upon by the body's response system advantageously as self. This will offer other therapeutic agents the opportunity to be looked upon as self in this delivery system and minimize adverse reactions and may herein and hereby be looked upon as self by the body's response system. Thus, in recapitulation and review the first component that is representative of subject composition L amino acid as well as being the product of the neutrophile enzymatic protective activity system now with these administered added dosages permits the neutrophile's inflammatory “friendly fire” to stop and the abnormal PCD inflammatory in vivo permeability test response, tracked by the radioactively tagged neutrophiles (as well as in vitro studies documenting antiinflammatory response of subject composition) now return to non-inflammatory normal tissue status and proceed to completion of the healing resolution cycle.

With stimulus switch-off signaling mechanism no new neutrophiles are stimulated to leave the bone marrow to enter the inflammatory PCD site tracked by permeability test (18 references) simultaneously with the need for response to tissue injury stimulus turned off the existing neutrophiles will migrate to the reticulo endothelial system sites as seen in the permeability studies (liver and spleen). Simultaneously again, with the autolytic enzymatic digestive response of the neutrophile silenced the tissue healing resolution to former integrity is initiated, again with the stimulus of the added dosages of L amino acid, Q1 01 KC by way of the law of mass action promoting stimulus for resynthesis of tissue protein.

Accordingly, 85% of the patients are symptom free within 4 weeks associated with normal radiographs of radio-actively tagged neutrophile permeability test (in contrast to abnormal radiographs prior to initiating free L amino acid Q1 01 KC subject composition therapy. This product is available on the market as infant formulation with 15.5% amino acids which composition is analogue and molar ratio analogue to human tissue and plasma and was specifically designed to mimic human holocrine tissue (in the form of breast milk whereby the entire cell contents of the mammary tissue is secreted). Available here with analogue to the immunologic concept of self, in the form of free L amino acid associated with high energy ionizable side chain groups available for tissue resynthesis to former integrity healing resolution of tissue.

Neutrophiles—Permeability

Lipopolysaccharides, a common neutrophile attractant, derived from and bacterial products such as bacterial endotoxins or exotoxins and may be deactivated by modification of HLB hydrophilic lipophilic balance by hydrophilic surfactant activity such as but not limited to the 8 propionic acid L amino acids (all but phenylalanine) of subject composition (other hydrophilic surfactants may be alternatively used such as but not limited to polysorbate 80, or sodium lauryl sulfate).

This application technology is made possible by the dramatic difference of L amino acids with a molecular weight of 100 or 200 vs. its parent molecule which can be exemplified by a molecular weight of 100,000. In which case 500 to 1000 alpha amino groups and in 500 to 1,000 carboxyl groups are now available in contrast to one alpha group and one carboxyl group in a parent printing molecule of 100,000 molecular weight. Dramatically illustrating the different reaction potentials now available with a therapeutic L amino acid subject composition. This same illustration is applicable for hydrophilic moieties and reactive side chain groupings as in the case said the seven propionic acids.

A biochemical therapeutic subject composition of essence of functional stem cell mimics embryonic stem cell with its pluripotent activity accelerates, facilitates, activates, stimulates, and evokes stem cell activity, and this therapeutic stem cell composition in tissue injury and disease mimics normal tissue, is present analog to human tissue and in analog molar ratios of human tissue and stimulates the suppression of inflammation, stimulates and promotes healing, and avoids per se their requirements are necessity of the introduction of foreign are nonself rejection and rejection like and linked components and adverse reactions thereof, is sourced from biochemical and immunological essence in common across species. While at the same time permits newly required medications to be utilized and protected in an envelope delivery system like mantle or cover including L amino acids and amino acid glycine as noncovalent bonding mechanism giving macromolecules such as DNA and protein shielding these medications from foreign and nonself haptene like recognition thereby greatly minimizing adverse reactions.

In animal husbandry we see an analog system or marker of immunologic self applied to springtime lambing. If a ewe or female sheep dies at birthing its offspring lamb, the chosen surrogate mother's placental blood is used as a marker for this orphaned newborn lamb for her to adopt, so that she will accept this newborn lamb as immunologic self and breast-feed it along with her own newborn lambs.

Analogue to this, in preparing donor organ for acceptance in transplantation, subject composition patient's blood may be used, as an organ bath and organ infusion to minimize rejection thereby as for example in CBA.

Therapeutic antiinflammatory activity is no longer present when presented as intact food such as the proteins of milk such as casein or whey. When free L and amino acids in this therapeutic composition are synthetically prepared analog to human tissue and analog to molar ratios of human tissue their function as significant anti-inflammatory agents suppressing cytokine stimulation of the inflammatory reaction and antagonist to the receptors of the inflammatory reaction results.

The biochemical essence and essence of function of stem cell such as but not limited to the exemplification and mimicking human tissue and protoplasm such as holocrine tissue such as but not limited to mammary tissue that pioneered cloning. L amino acids analog to human tissue and analog molar ratio synergistically combining further with the first extracellular matrix biochemical muco-polysaccharide produced by cleavage of the fertilized ovum as embryonic stem cell and further synergistically combined with phospholipid (self vesiculating essence of cell membrane).

These free L amino acids and their reactive sidechain groupings and ionizing groupings are also analog to the synthetic therapeutic (therapeutically active mainstay of PCD) amino acid five ASA and active anti-inflammatory component of sulfasalazine exemplified by tyrosine and its phenolic hydroxyl groupings along with synergistic effect of acetyl grouping of glycine completing the functional and structural grouping anti-inflammatory tissue healing analog. Simultaneously the same L amino acids tyrosine and its phenolic hydroxyl grouping co-analogs to the propionic acid derivative anti-inflammatory drugs such as ibuprofen and naproxen and their distinguishing acyl side grouping and is in these L amino acids are also on its alpha (second) carbon acyl grouping representing the high-energy alpha amino grouping in the case of the L amino acids.

It will be recalled that all amino acids are ordinary organic acids which have an amino grouping in the molecule. It will also be recalled that the second carbon atom, which is also next to the carboxylic acid group is called the alpha carbon atom. This is also exemplified by tyrosine, cited here, as one of the 8 propionic acid derivative L amino acids.

Further exemplified such as but not limited to analog to acetyl salicyclic acid with the analog acetyl reactive sidechain grouping of the acetyl grouping of alpha amino acetic acid of glycine alone with the hydroxylphenolic grouping of tyrosine. This is further exemplified metabolically and pharmacodynamically and pharmacokinetically such as but not limited to glycine conjugate intermediary metabolites of acetyl salicyclic acid.

To make this subject composition more palatable, in fact even pleasant tasting per taste panel review—and therefore overcoming the very unpalatable taste that has led to 15 to 20% non-compliance and the requirement of a nasogastric tube to administer this very beneficial anti-inflammatory, anti-rejection stimulating, facilitation, accelerating, synergizing, healing tissue protein synthesis therapy. In the management of one of the most resistant, fraught with complications such as, but not limited to, Crohn's disease. Use of subject composition in congenital biliary atresia enables bringing about the reversal of these diseases with subject composition. in these cases as far as the non-compliance patients are concerned, the advances in flavor are as important as the advances in the product.

This savoring flavor may also include and may be obtained by flavors such as, but not limited to, savoring soup flavors such as but not limited to, vegetable soup, asparagus soup, broccoli soup, cucumber, and celery and/or pea soup, beef, fish and seafood. The concentrated flavor as found in a bullion cube, as found in Wyler's granules chicken flavor, Borden's Foods Corp. Columbus, Ohio for this application technology.

The required dosage (5 gm. To 15 gm) was mixed in a in water that had been pre-warmed (luke warm, with a drop test on the forearm) spring or distilled water, in the microwave oven for approximately 35 seconds together with ⅓ or ½ of a 4 gram bullion cube (chicken in this example) resulted in a creamy chicken soup flavor. This flavor system addresses the compliance issue and therapeutically successful use of subject composition in Crohn's disease as cited in previous embodiments. Such Crohn's disease patient has continued to do well with this pleasantly flavored subject a composition.) Bullion cube utilized, Hormel brand, Austin, Minn.

Subject composition and all its components and therapeutic stem cell components including but not limited to components that stimulate, facilitate, accelerate and synergize in vivo including but not limited to human and also applicable to all mammalian stem cell. Subject composition included here by reference of patent application Ser. No. 09/629,859 including L amino acids and glycine, phospholipids such as but not limited to phosphatidylcholine, extracellular matrix such as but not limited to collagen, including the collagen subtypes of vertebrates but not limited to collagen I to X, fibronectin and its collagen specific protective effects (from collagenase) binding sites, including but not limited to other collagenase inhibitors such as alpha 2 macroglobulin and beta I macroglobulin, chondroitin sulfate, glucosamine, mucopolysaccharides, mucoproteins, elastin, the components of basement membrane including but not limited to collagen type IV, laminin, entactin, heparin sulfate with its characteristic high anionic charge surfactant activity playing a major role in glomerular filtration.

A remarkable amount of tissue organization of subject composition and its components that has been downloaded into, for example but not limited to, the extracellular matrix components of subject composition (growth factors are commonly enmeshed and interwoven in extracellular matrix or maybe optionally added in specialized therapeutic use of subject composition, and (exemplified in Table 4), making it invaluable in subject composition use and unique therapeutic use for disease and wound tissue healing and tissue reformation, tissue protein synthesis in conjunction with other viable therapeutic usages such as but not limited to anti-inflammatory effects, a rejection activity, reversal of disease systemic effects and illustrated and exemplified in such as but not limited to growth and puberty impairment in pediatric Crohn's disease reversal of sedimentation rate C-reactive protein, averting the need for liver transplant in congenital biliary atresia and many other embodiments. All illustrating the stem cell activity and stimulation of subject composition in the therapy of disease.

The effects of biochemical essence of human stem cell and the effect of mimicking and analog to human tissue can be seen in cells of the epidermis retaining their stem cell character as long as they are attached to basement membrane components. Chondrocytes in cartilage production remain active as long as they are in contact with the stimulus of collagen and cartilage specific proteoglycans. The prior art has not taught the use of subject composition and its components as a stem cell therapeutic agent analog and mimicking embryonic stem cell tissue as presented in these embodiments to become available as a therapeutic pharmaceutical agent. Nor has it been taught that the additional value of noncovalent bonding into further mimicking and analogue to the most important bonding technique used in human tissue by the body because of no restricted limitation of prompt exchange promulgated by non covalent bonding therefore the valued multiplicity of efficacious therapeutic uses with minimal if any side effects. At the same time as synergizing these many effects and the effects of co-use with covalent and valently bonded medications from examples such as but not limited to antibiotics in major infections with associated severe inflammatory changes, to insulin in the management of diabetes with associated severe inflammatory changes and great need for tissue healing such as but not limited to progressively severe atherosclerosis and debilitating complicating changes, additionally synergized by the following further HLB modulation that may be optionally included in subject composition(s):

1. The noncovalent further bonding with phospholipids and required HLB modulation can be further illustrated by the advantageous use of hydrophilic surfactants reaching an HLB of 18 to 20 such as but not limited to Tween 60, and sodium lauryl sulfate respectively as therapeutically applied to antibiotics or used in conjunction with antibiotics (these surfactants may be applied locally and/or systemically for a systemic infection and/or systemically for, but not limited to a systemic infection) in the treatment of resistant infections such as but not limited to gram negative E. coli with its own outer bacterial protective fatty cell membrane component covering that makes it gram negative and antibiotic resistant and/or similar use with insulin in associated lipid diseased metabolism. Phospholipids such as phosphatidyl choline and HLB of two, PGPR can be added to synergize prior dispersion of the fat and make it more available for further synergistic foregoing action of highly hydrophilic surfactants.

2. These foregoing therapeutic components and progressive steps of subject composition may be similarly applied to other diseases with disturbance in fat metabolism such as, but not limited to, cystic fibrosis synergizing its inadequate lipase activity, and in the rare Gaucher's disease a lipid storage disease of glycolipid cerebroside with its characteristic foam cells may be helped in a similar sequential HLB treatment fashion or perhaps, with hydrophilic surfactant alone. Thereby so emulsifying the fat into very small particles of fat, which more readily fit into the 3D lipase enzymatic molecular clefts in metabolizing the fatty plaques even with excess of fat or deficiency of enzyme or excessive enzyme inhibitor (appropriate enzyme inhibitor modulation and/or additions of appropriate enzymes may be optionally added to subject composition).

3. The same principle as applicable to any enzyme deficiency quantitatively or qualitatively as in the uncommon lysosomal storage diseases in this case lipid storage disease such as, but not limited to, Nieman Pick deficiency of sphingomyelinase and therefore an abnormal accumulation of sphingomyeiln in vital organs resulting in disease occurs.

4. Other similar deficiencies in enzymes result in, storage disease is included glycogen storage disease such as Pompe disease, other rarer lipid storage disease sphingolipidoses such as but not limited to Tay Sachs disease, as sulfatidosis such as but not limited to Fabry disease and includes Gaucher disease and Nieman-Pick disease mucopolysaccharidosis such as Hurlers disease, mucolipidosis such as but not limited to pseudo-Hurler disease. All of these storage disease represent and result from an impairment in metabolism a commonality of all plaque like diseases another commonality is poor solubility and poor solubilization but also represented by the prion diseases in animals and humans, Alzheimer's disease, with plaque-like microscopic cerebral tangles, and even more commonly represented by atherosclerosis and its associated poorly metabolizable lipid plaque. Another diverse example of this principle is asbestosis where the asbestos is not only poorly combustible and there for used as fireproofing but also poorly combustible from the metabolic standpoint. Plaque-like diseases may be grouped and looked upon as a poorly soluble bone stuck in the throat of diseased metabolism.

5. All these diseases may be given as a therapeutic opportunity for reversibility to more normal state by the above suggested modulation of HLB with highly hydrophilic surfactants of HLB of 18 to 20 such as but not limited to Tween 80 and sodium lauryl sulfate preceded by lipophilic surfactant for lipid dispersion such as extreme lipophilic HLB surfactant of 2 as in the case of PGPR which may be accompanied by the surfactants found in lecithin such as, but not limited to, phosphatidyl choline. With neurologic involvement phosphatidyl inositol also should be included which has an application affinity and efficacy for the nervous system which should also be utilized as a representative of a lecithin derived polar active surfactant in addition to the foregoing therapeutic efforts, which may be optionally included in the subject composition, to reverse these plaque-like disease states.

The major lipid components of biological cell membranes include but are not limited to glycerophospholipids, sphingolipids, glycosphingolipids, and glycoglycerolipids as the components of the subject composition.

The most common phospholipid applied to vesiculation of cell membrane of subject composition, analogue and mimicking human tissue is phosphatidyl choline but specific therapeutic variations may be necessary as required by disease and disease site such as dipalmatylphosphatidyl choline, a natural surfactant of the lung such as, but not limited to, its application in atalectasis in the infant or adult, and may in this instance occupy as much as 50% or more of the total phosphatidyl choline. In the case of biliary tract disease and gallstones diacyl-phosphatidyl choline. In the case of the erythrocyte disease, the use of dipalmatylphosphatidyl choline, again mimicking and analogue to the phosphatidyl choline of normal erythrocytes. The kidney and heart are made up of both diacyl and alkenylacyl phosphatidyl choline.

Other examples such as, but no limited to the liver, show that more than 20 molecular species of phosphatidyl choline have been identified and, therefore, applicable to subject composition. Adipose tissue, palmitoyl stearoyl oleates and linoleates show variations in subject composition and may be necessary in this therapeutic disease application for subject composition.

Table 5 enclosed to illustrate variations in phospholipid and other polar lipids applicable in subject composition, e.g. the second carbon of phosphatidyl choline is usually unsaturated and the first carbon is saturated fatty acid component, but this may be reversed. The phospholipids are usually of seed oil origin but may also be derived from animal tissue origin e.g. but not limited to fish oil. After the omega-3 anti-inflammatory fish oil source, (anti-prostaglandin one and three) fish oils are extracted, the 60 percent residual lipid now available can be degummed as a source of phospholipid membrane surfactant with yet another pharmaceutical activity omega-3 anti-inflammatory activity can be covalently present at (or may be used non-covalently as in embodiments of subject composition in patent application Ser. No. 09/639,859, hereby incorporated by reference in its entirety). This combined pharmaceutical efficacy may also be accomplished by covalently bonding for example but not limited to esterification of phospholipid cell membrane lysolecithin (produced from fish or seed oil sources) pharmaceutical activity with fish oil or seed oil source anti-inflammatory omega-3 fatty acid activity again analogue to and mimicking human tissue.

Other extracellular matrix components or components that interact with extracellular matrix may be included in the subject composition (again analogue to and mimicking human tissue):

1. Intact basement membrane and its components are considered important in the prevention of the invasion and metastatic invasive spread of diseases such as but not limited to cancer in preventing the spread of cancer to the extracellular matrix and into the bloodstream. Transmembrane cadherins, a calcium dependent family of adhesion molecular glycoproteins whose loss of function has been associated with cancer metastasis and to be considered for inclusion in subject composition in helping with this disease of very poor prognosis.

2. Classic cadherins (E epithelial, N neural, P placental respective cell sites of origin) complex with cytoplasmic proteins known as catenins anchoring them to the attn based cytoskeleton required for adhesive function. Desmocollins and desmogleins differ from the classic family cadherins by the structure of the cytoplasmic domain.

3. The structural glycoproteins such as fibronectin one of the first macro molecules deposited in embryonic stem cell activity in embryonic development and similarly active in the wound healing of many embodiments and looked upon as a recapitulation of embryonic stem cell activity. Because of the fibronectin bonding capacity and specialized binding sites it connects cellular and other components of the extracellular matrix into functional units along with collagen type III is therefore important in tissue healing in wounds and disease. Collagen, fibronectin. along with laminin, are the first to be deposited as extracellular matrix by embryonic stem cell in the fertilized ovum stage and parallel their importance in healing wounds and disease tissue used here in subject composition analogue to and mimicking human tissue (as well as all extracellular matrix components to follow).

4. These adhesive glycoproteins (analogue to and mimicking human tissue) making one extracellular matrix component combined to another and to cells, in this function also include the integrins. Fibronectin molecules binds avidly to collagen, proteoglycans, glycosaminoglycans, fibrinogen, fibrin, cell surface, bacteria and DNA. Fibronectin is ubiquitous in the extracellular matrix found in the delicate filaments, as small aggregates, attached to collagen fibers on cells surfaces, a him and may be trapped in basement membranes such as the glomerular filter. Another extracellular matrix glycoprotein is osteonectin and another homologous glycoprotein SPARC (protein rich L cysteine amino acid) also found in some basement membrane. Osteopontin and osteocalcin are other glycoproteins found in osseous tissue.

5. Analogue to and mimicking human tissue for subject composition and for optional subject composition inclusion: Proteoglycans are found widely distributed on cells surfaces, biologic fluids and in all extracellular matrices. As organizers of the extracellular matrix they are deposited early in wound healing even before collagen so important in the disease and tissue heating function and structure of many embodiments presented here. Some of the most common proteoglycans, such as but not limited to heparan sulfate, chondroitin sulfate and dermatan sulfate, their polysaccharide polymer component glycosaminoglycans (contain an amino sugar) were formerly called mucopolysaccharides and their high-grade gels maintain tissue turgor. They participate in the organization of extracellular matrix by binding to collagen₅ elastic fibers and fibronectin. In wounds and disease healing the collagen fibers provided tensile strength, interwoven with elastin limit the elasticity of elastin, which has the ability to recoil after stretching as provided by the elastin glycoproteins rich in lysine and proline like collagen but unlike collagen elastins contains no hydroxylated amino acids.

6. Elastlin's molecular cross-links form an extensive network and random coils (rather than definitive proteins folds oscillating between different states and form the random folds) determine their capacity to stretch and recoil. It is evident that many components of extracellular matrix such as but not limited to, elastin are enmeshed and entwined in extracellular matrix products analogue to and mimicking human tissue included in subject composition such as generic capsules or liquid of shark or beef (such as but not limited to tracheal cartilage) collagen, chondroitin sulfate to be included in subject composition. The elastin (available such as, but not limited to, generic porcine aortic powder) to be included in subject composition in the therapeutic management of cardiovascular disease and vascular disease, including the in vitro growth of heart valves for potential replacement in contrast to porcine valves in vascular diseases such as but not limited to congenital heart disease, atherosclerotic aortic stenosis and aortic lesions such as but not limited to the management of Marfans syndrome, elastin deficiency, subject compositions so enriched with elastin also subject composition may be similarly adapted as in foregoing examples, and made applicable to skeletal diseases such as but not limited to those caused by Marfan syndrome.

7. Other components interacting with extracellular matrix including, but not limited to, actin, talin, vinculin, is paxillin, alpha actin, tensin, kinase.

8. Included in the molecular components of subject composition are the polypeptide growth factors listed in and included in Table 4 the two and includes tables and may be enmeshed in the extracellular matrix with its significant downloaded software computer-like information for example but not limited to EGF/TGF alpha with its embryonic stem cell like function (has been added in experimental animal stem cell studies to cause precocious tooth eruption and eyelid opening in animals).

9. Fibroblast growth factor, FGP plays a significant role in wound repair and can associate with heparan sulfate in the extracellular, matrix serving as a reservoir for growth factor controlling cell proliferation. Three tables enclosed in the illustration page entitled “Table 4” factors in wounds and disease healing.

In the processing presented in several embodiments of pathogens and minimizing reactive pathogenic effects as in the case of, such as, but not limited to: proteins as allergens in allergic diseases, potential side effects of were foreign proteins in vaccine production, abnormal prion proteins as in Mad Cow or the human equivalent disease modification whether by removal of potentially contaminated bovine liquid products such as milk with ultrafiltration, or 3D spatial protein modification by processing as applied to such potential products, but not limited to, meat that might possibly derive from cow in areas where mad cow disease is epidemically suspected, with supercritical carbon dioxide, liquid nitrogen, urea or guanidine treatment of 3D spatial modification of proteins analogue and mimicking heat denaturation of a protein with the quantitative change and qualitative change in structural and functional capacity in contrast to former pathogenic states are measurable and of utmost importance in the comparative reporting as applied to safer consumer use and consumer exposure. This can be exemplified but not limited to any of the above treatments resulting in a product tolerated by the moderately allergic patient with a 90 to 99 percent reduction of the pathogenicity and pathogenic reactive potential, such as but not limited to, the reduction of allergenicity as required for the prevention of severe allergic reactions in the exquisitely hypersensitive allergic patient where one nanogram or even one picogram or even tenfold 100 fold or one thousand fold less than that, might be approaching very practical limit of tolerance for this extremely allergic patient.

In the United States about 2000 such severe reactions are reported yearly, e.g., anaphylaxis to milk, and are included in the medical categorical description as but not limited to anaphylaxis.

EXAMPLE 1

Whey diluted 20% with spring water was filtered through a tubular spiral wound membrane ultrafilter (0.01 μm pore size). The permeate (pH 6.6) was immediately batch pasteurized at 145° F. for 30 minutes, followed by refrigeration. Reexamination of the pH and titratable acid revealed no decrease in pH or increase in acid after 7 days of refrigeration.

EXAMPLE 2

Several six-ounce glasses of the refrigerated permeate of Example 1 were flavored with 12 ml (corresponding to 5%) of one of the following flavor concentrates: banana, hypoallergenic low acid orange, hypoallergenic chocolate flavor, or tropical fruit. In another experiment, 30 ml of non-concentrated pear nectar was added to 70 ml of refrigerated permeate. A taste panel found all these products to be pleasant tasting, very palatable, bland and not salty.

EXAMPLE 3

The liquid permeate of Example 1 was dried to a moisture content of about 4 wt % by spray-drying, employing a dryer inlet temperature of 400° F. and a dryer outlet temperature of 200° F., with a drying time of 4 hours, at a pressure of 2500 psi, and a 68 gauge spray nozzle bore. Two 50 lb samples of dried permeate were produced in this manner. The dried permeate was then reconstituted to its native liquid form by combining 6.2 weight parts of powder with 93.8 weight parts of water.

EXAMPLE 4

The powdered permeate of Example 3 was reconstituted in flavored soda by adding 3 weight parts of flavored soda to 7 weight parts of powdered permeate.

EXAMPLES 5 TO 6

To 100 ml of the reconstituted liquid permeate and permeate-soda of Examples 3 and 4 was added one drop of lactase. The samples were stored for 24 hours in a refrigerator to permit the lactase to act on lactose in the samples, resulting in the production of the monosaccharides glucose and galactose which sweetened the product.

EXAMPLE 7

Seventy ml of the reconstituted liquid permeate prepared according to Example 3 is diluted with 30 ml water to achieve a potassium level of about 25 mEq/L. To the 100 ml sample is then added the following: 2 mEq NaCl and 1 mEq sodium citrate. This increases the sodium level of the sample to 45 mEq/L from the estimated natural level of 15 mEq/L, and increases the citrate level to 29 mEq/L from the estimated natural level of 19 mEq/L. The addition of the NaCl also increases the chloride level from 18 to 38 mEq/L. Upon addition of flavoring, the product may be used as an electrolyte beverage to replace fluid or electrolytes lost from diarrhea.

EXAMPLE 7a

To the electrolyte beverage of Example 7 was added 3.5% finely milled and sifted rice flour to augment the taste of the electrolyte solution.

EXAMPLE 7b

1 gram of essentially fat-free (less than 1 wt % fat) cocoa powder (prepared by supercritical CO₂ treatment of cocoa powder) was added to 100 ml of the beverage prepared according to Example 7 to form an electrolyte fluid replacement liquid drink. One drop of lactase enzyme was then added to convert the lactose to component monosaccharides.

EXAMPLE 8

1 gram of essentially fat-free (less than 1 wt % fat) cocoa powder (prepared by supercritical CO₂ treatment of cocoa powder) was added to 100 ml of liquid permeate prepared in accordance with Example 1, diluted 90% with water to achieve a potassium level of 3 mEq/L. One hundred mg of NaCl was then added to achieve a sodium level of 19 mEq/L and a chloride level of 20 mEq/L. Fructose was added in the amount of 4.5 g to bring the carbohydrate level to 5%. The result was a chocolate-flavored electrolyte fluid replacement drink also useful as a sports drink.

EXAMPLE 8a

One gram of essentially fat-free (less than 1 wt % fat) cocoa powder prepared by supercritical CO₂ treatment of cocoa powder was added to the beverage of Example 8, along with 2% finely milled and sifted rice flour to augment the taste of the sports exercise drink.

EXAMPLE 8b

To 100 ml of the exercise drink of Example 8a was added 1 drop of lactase enzyme preparation, followed by refrigeration for 24 hours to convert the lactose to its component monosaccharides, namely, glucose and galactose. The conversion of lactose augmented the taste of the beverage.

EXAMPLE 9

A hypoallergenic milk product was prepared as follows. To 250 ml of the liquid permeate prepared according to Example 1 was added 3.5% oat soy powder, 0.5% deproteinized anhydrous oil rendered hypoallergenic in accordance with U.S. Pat. No. 5,112,636, 0.05% vitamin E as an antioxidant and 1.8% finely milled and sifted rice flour.

EXAMPLE 9a

The procedure of Example 9 was repeated except that the amounts of finely milled and sifted rice flour was increased to 3.5%, and 1% supercritical CO₂-defatted chocolate flavor was added.

EXAMPLE 10

0.62 grams of dried whey permeate was added to 50 ml of diet non-phosphate cream soda and 50 ml of non-phosphate cream soda to achieve a fructose concentration (fructose is the carbohydrate in the soda) to 6.0%. To this was added 100 mg of NaCl to achieve a sodium ion concentration of 19 mEq/L (45 mg %) and a chloride level of 20 mEq/L. The beverage is useful as a sports exercise drink.

EXAMPLE 10a

One gram of essentially fat-free (less than 1 wt % fat) cocoa powder prepared by supercritical CO₂ treatment of cocoa powder was added to the beverage of Example 10, along with 2% finely milled and sifted rice flour to augment the taste of the exercise drink. The beverage is also an instant soda fountain drink.

EXAMPLE 10b

To 100 ml of the exercise drink of Example 10a was added 1 drop of lactase enzyme preparation, followed by refrigeration for 24 hours to convert the lactose to its component monosaccharides, namely, glucose and galactose. The conversion of lactose augmented the taste of the beverage.

EXAMPLE 11

Example 10 was repeated, deleting the 50 ml of diet soda and increasing the amount of non-diet soda to 100 ml, to achieve a pleasantly flavored hypoallergenic sports exercise dring beverage having a carbohydrate content of 11%.

EXAMPLE 11a

To 100 ml of the beverage of Example 11 was added 1 gram of essentially fat-free (less than 1 wt % fat) cocoa powder prepared by supercritical CO₂ treatment of cocoa powder. Also added was 2% of finely milled and sifted rice flour to augment the taste of the beverage.

EXAMPLE 12

An elemental sports exercise drink is prepared as follows. To the composition of Example 10b is added 0.5% of an amino acid mixture containing less than 0.25% protein, preferably less than 0.025% protein.

EXAMPLE 13

An electrolyte replacement beverage is prepared by adding to the composition of Example 70.5% of an amino acid mixture containing less than 0.25% protein, preferably less than 0.025% protein. APPENDIX 1 NEOCATE Ingredients Per 100 Per Quart kcal Per 100 G (32 fl:oz) Calories 100 420 640 Amino Acids, g 3.7 15.5 23.6 (Protein Equivalent, g) 3.1 13 19.8 Fat, g 4.5 19.1 29 Carbohydrate, g 11.7 49.3 74.9 Water, g 131 550 840 Linoleic Acid, mg 677 2850 4332 VITAMINS Vitamin A, IU 409 1721 2616 Vitamin D₃, IU 87 366 556 Vitamin E, IU 1.14 4.8 7.3 Vitamin K, mcg 8.79 37 56 Thiamin, mcg 92.6 390 593 Riboflavin, mcg 137.8 580 882 Vitamin B₆, mcg 123.5 520 790 Vitamin B₁₂, mcg 0.17 0.7 1.1 Niacin, mg 1.54 6.5 9.88 Folic Acid, mcg 10.2 43 65 Pantothenic Acid, mg 0.62 2.61 3.97 Biotin, mcg 3.1 13 20 Vitamin C, mg 9.26 39 59 Choline, mg 13.1 55 84 Inositol, mg 23.3 98 149 MINERALS Calcium, mg 124 522 793 Phosphorous, mg 93.1 392 596 Magnesium, mg 12.4 52 79 Iron, mg 1.85 7.8 11.9 Zinc, mg 1.66 7 10.6 Manganese, mcg 90 380 578 Copper, mcg 124 520 790 Iodine, mcg 15.4 65 99 Molybdenum, mcg 4.75 20 30 Chromium, mcg 3.56 15 23 Selenium, mcg 3.73 15.7 23.9 Sodium, mg 37.3 157 239 Potassium, mg 155.1 653 993 Chloride, mg 77.2 325 494 INGREDIENTS: Corn Syrup Solids (55.9%), Hybrid Safflower Oil (11.2%), Refined Vegetable Oil (Coconut 6.1%, Soy 3.1%), L-Lysine L-Glutamate (2.8%), Calcium Phosphate Dibasic (2.4%), and less than 2% of each of the following: L-Leucine, Tripotassium Citrate, L-Proline, L-Arginine, L-Valine, L-Aspartic Acid, L-Isoleucine, Glycine, L-Threonine, L-Tyrosine, L-Phenylalanine, L-Serine, L-Histidine, L-Alanine, Mono and Diglycerides, Sodium Chloride, L-Cystine, # L-Tryptophan, Magnesium Acetate, L-Methionine, Potassium Chloride, Diacetyl Tartaric Acid Esters of Monoglycerides, L-Glutamine, Choline Hydroxide, L-Glutamic Acid, M-Inositol, Soy Lecithin, Tricalcium Phosphate, Ascorbic Acid, Ferrous Sulfate, Zinc Sulfate, Taurine, L-Carnitine, Niacinamide, DL-alpha Tocopheryl Acetate, Calcium Pantothenate, Cupric Sulfate, Manganese Sulfate, Pyridoxine Hydrochloride, Vitamin A Acetate, Riboflavin, Thiamine Chloride # Hydrochloride, Potassium Iodide, Chromium Sulfate, Phylloquinone, Sodium Molybdate, Folic Acid, Sodium Hydrogen Selenite, Biotin, Vitamin D3 and Cyanocobalamin.

TABLE 1 Average composition of milk (100 g) of 4 species [26] Ewes Goats Cows Human Solids, total % 19.30 12.97 12.01 12.50 Energy, kcal 108 69 61 70 KJ 451 288 257 291 Protein, total 5.98 3.56 3.29 1.03 Lipids, total % 7.000 4.14 3.34 4.38 Carbohydrates, % 5.36 4.45 4.66 6.89 Ash, % 0.96 0.82 0.72 0.20 Ca, mg 193 134 119 32 Fe, mg 0.10 0.05 0.05 0.03 Mg, mg 18 14 13 3 P, mg 158 111 93 14 K, mg 136 204 152 51 Na, mg 44 50 49 17 Zn, mg — 0.30 0.38 0.17 Ascorbic acid, mg 4.16 1.29 0.94 5.00 Thiamin, mg 0.065 0.048 0.038 0.014 Riboflavin, mg 0.355 0.138 0.162 0.036 Niacin, mg 0.417 0.277 0.084 0.177 Panthothemc 0.407 0.310 0.314 0.223 acid, mg Vitamin B6, mg — 0.046 0.042 0.011 Folacin, mcg — 1 5 5 Vitamin, B12, mcg 0.711 0.065 0.357 0.045 Vitamin A, RE 42 56 31 64 IU 147 185 126 241 Saturated FA, g 4.60 2.67 2.08 2.01 C4:0, g 0.20 0.13 0.11 — C6:0, g 0.14 0.09 0.06 — C8:0, g 0.14 0.10 0.04 — C10:0, g 0.40 0.26 0.08 0.06 C12:0, g 0.24 0.12 0.09 0.26 C14:0, g 0.66 0.32 0.34 0.32 MCT total (C6-C14), g 1.58 0.89 0.61 0.64 C16:0, g 1.62 0.91 0.88 0.92 C18:0, g 0.90 0.44 0.40 0.29 Monounsat, FA, g 1.72 1.11 0.96 1.66 C16:1, g 0.13 0.08 0.08 0.13 C18:1, g 1.56 0.98 0.84 1.48 C20:1, g — — trace 0.04 C22:1, g — — trace trace Polyunsat, FA, g 0.31 0.15 0.12 0.50 C18:2, g 0.18 0.11 0.08 0.37 C18:3, g 0.13 0.04 0.05 0.05 C18:4, g — — trace — C20:4, g — — trace 0.03 C20:5, g — — trace trace C22:5, g — — trace trace C22:6, g — — trace trace Cholesterol, mg — 11 14 14 Phytosterol, mg — — trace — L Amino Acids: Tryptophan, g 0.084 0.044 0.046 0.017 Threonine, g 0.268 0.163 0.149 0.046 Isoleucine, g 0.338 0.207 0.199 0.056 Leucine, g 0.587 0.314 0.322 0.095 Lysine, g 0.513 0.290 0.261 0.068 Methionine, g 0.155 0.080 0.083 0.021 Cysteine, g 0.035 0.046 0.030 0.019 Phenlyalamne, g 0.284 0.155 0.159 0.046 Tyrosine, g 0.281 0.179 0.159 0.053 Valine, g 0.448 0.240 0.220 0.063 Arginine,g 0.198 0.119 0.119 0.043 Histidine, g 0.167 0.089 0.089 0.023 Alanine,g 0.269 0.118 0.113 0.036 Aspartic acid, g 0.328 0.210 0.250 0.082 Glutamic acid, g 1.019 0.626 0.689 0.168 Glycine, g 0.041 0.050 0.070 0.026 Prolme, g — 0.368 0.319 0.082 Serine, g 0.492 0.181 0.179 0.043

TABLE 2 Relative composition of ewe and goat milk in relation to the composition of human milk = 100% [26] Ewe Goat Cow Solids, total 154 104 96 Energy 154 99 87 Protein 580 346 319 Fat 160 94 76 Lactose 78 64 68 Minerals 480 410 360 Ca 603 419 372 Fe 333 167 167 Mg 600 457 433 P 1128 793 664 K 267 400 298 Na 259 294 288 Zn N/A 176 224 Ascorbic acid 83 26 19 Thiamin 464 343 271 Riboflavin 986 383 450 Niacin 236 156 474 Pantothenic acid 182 139 141 Vitamin B6 N/A 418 382 Folacin N/A 20 100 Vitamin B12 1580 144 793 Vitamin A 65 88 48 Saturated fatty acids 229 133 103 C4:0 butyric 2000 1300 1100 C6:0 caproic 1400 900 600 C8:0 caprylic 1400 1000 400 C10:0 capric 667 433 133 C12:0 lauric 92 46 35 C14:0 myristic 206 100 106 C16:0 palmitic 176 99 96 C18:0 stearic 310 152 138 Monounsaturated FA 104 67 58 C16:1 palmitoleic 100 62 62 C18:1 oleic 105 66 57 Polyunsaturated FA 62 30 24 C18:2 linoleic 49 30 22 C18:3 linolenic 260 80 100 MCT-FA C6:0-C12:0 288 178 84 Cholesterol N/A 79 100 Tryptophan 494 259 270 Threonine 583 354 324 - Isoleucine 604 370 355 -. Leucine 618 330 339 Lysine 754 426 384 - Methionine 738 381 395 Cysteine 184 242 158 . Phenylalanine 617 337 346 . Tyrosine 530 338 300 - Valine 711 381 349 Arginine 460 277 277 Histidine 726 387 387 - Alanine 747 328 314 Aspartic acid 400 256 305 Glutamic acid 606 373 410 - Glycine 158 192 269 . Proline N/A 449 389 Serine 1144 421 416 - = cyclosporin analog of utility patent . = yogurt and amino acids

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A is a schematic drawing of the phases of mitosis. Similar to reversed hexagonal phase low HLB colloid micelle (lipophilic=hydrophobic phase of surfactant effect). Factors of mitosis include genetic distribution, mobilization of membrane of cell, cell nuclei, and intranuclear phospholipids.

FIG. 1B shows cerebrospinal fluid showing metastatic breast cancer cells and abnormal mitosis (mitotic figures) of cancer.

FIG. 2 is a schematic of surfactant forces in emulsions. It shows the typical sequence of phases that develops when a surfactant is mixed with water. Hydrophilic surfactant as high HLB of 18 of Tween80. Lipophilic(hydrophobic)low HLB surfactants (e.g. lecithin 4 to 7). Cancer appears as an uncontrolled phase equivalent in its extensive mitosis to lipophilic reversed hexagonal phase micelle.

FIG. 3 is a schematic of different kinds of surfactant aggregation.

FIG. 4 is a graphical representation of the amount of histamine released in response to different dilution factors of the treatment to reduce the allergenicity of cat dander.

FIG. 5A shows the structural formula of phosphatidyl choline (PC).

FIG. 5B shows the structural formula of phosphatidyl sarine (PS).

FIG. 5C shows the structural formula of phosphatidyl ethanolamine (PE).

FIG. 5D shows the structural formula of N-Acylphosphatidyl ethanolamine (NAPE).

FIG. 6A shows the structural formula of phosphatidyl inositol (PI).

FIG. 6B shows the structural formula of phosphatidyl glycerol (PG).

FIG. 6C shows the structural formula of phosphatidic acid (PA).

FIG. 6D shows the structural formula of plasmogen, wherein X=choline or ethanolamine.

FIG. 6E shows the structural formula of diphosphatidyl glycerol (DPG).

FIG. 7A shows the structural formula of ibuprofen.

FIG. 7B shows the structural formula of fenoprofen.

FIG. 7C shows the structural formula of naproxen.

FIG. 7D shows the structural formula of ketoprofen.

FIG. 7E shows the structural formula of flurbiprofen.

FIG. 8 shows the mechanism of membrane damage in ischemia and reperfusion.

FIG. 9A shows the structural formulas of several para-aminophenol derivatives.

FIG. 9B is a schematic drawing of the antipyretic action of acetaminophen. Similar biochemical groupings, the amino and phenol moieties as in tyrosine and down regulation IL1/TNF and IL6 as a anti-inflammatory component of the subject composition.

FIG. 10A shows a low power micrograph of the pathology of Crohn's disease. Extensive pathologic changes normalized in 2-4 weeks with therapeutic subject composition.

FIG. 10B shows Crohn's disease granuoloma of the colon. Extensive pathologic changes normalized in 2-4 weeks with therapeutic subject composition.

FIG. 11A shows Indium III Abnormal radiogram of ileal inflammation.

FIG. 11B shows a normalized Ileum 4 weeks after treatment with therapeutic subject composition.

FIG. 12 is a schematic drawing of a liver illustrating the locus of congenital biliary atresia disease being close to the location of stem cells and in approximately the area of believed therapeutic activity. Biliary atresia is evidenced by a sheet of periductular inflammation and fibrosis. Extensive periductule inflammation as seen on this H and E slide. This inflammatory obstruction also prevents reanastomosis of the biliary ductules diagrammatically illustrated here by superimposing the histopathology of biliary atresia upon the normal microscopic anatomy of the liver.

-   -   1. Locus (location)—See text     -   2. Hepatic Artery     -   3. Portal Vein     -   4. Bile Duct     -   5. Locus (location)—See text     -   6. To Hepatic Veins and inferior Vena Cava     -   7. Sublobular Vein to Hepatic Veins and Inferior Vena Cava     -   8. Central Vein     -   9. Sinusoid     -   10. Interlobular Vein 

1.-33. (canceled)
 34. A composition for treatment of damaged tissue comprising: a. amino acids or salts thereof present at a molar ratio which is characteristic of sheep milk or goat milk; b. at least one essential lipid; c. at least one protective antioxidant lipid; and d. at least one mucopolysaccharide.
 35. A composition comprising: a. amino acids present at a molar ratio which is characteristic of sheep milk or goat milk; and b. at least one essential lipid.
 36. The composition of claim 35, further comprising chondroitin sulfate and eicosapentanoic acid.
 37. A composition comprising: a. amino acids present at a molar ratio which is characteristic of sheep milk or goat milk; b. at least one lipid; c. at least one mono- or di-saccharide sugar; d. at least one vitamin; e. at least one mineral; and f. at least one antioxidant.
 38. The composition of claim 34, further comprising collagen.
 39. The composition of claim 34, wherein the at least one mucopolysaccharide is chondroitin sulfate.
 40. The composition of claim 34, wherein the at least one protective antioxidant lipid is eicosapentanoic acid.
 41. The composition of claim 36, further comprising collagen.
 42. The composition of claim 35 wherein the essential lipid comprises a fatty acid.
 43. The composition of claim 35 wherein the essential lipid comprises a phospholipid.
 44. A mucosal delivery system for delivering an antigen or drug to a patient or animal, the mucosal delivery system comprising: a chylomicron vehicle having a diameter ranging from about 0.5 microns to about 1 micron, the chylomicron vehicle comprising: a. liquid fat from an oil selected from the group consisting of palm kernel oil, coconut oil, corn oil and mixtures thereof; and b. at least one surfactant selected from the group consisting of polyglycerol polyricinolate, phosphatidylcholine, glycerine and polysorbate
 80. 45. The mucosal delivery system according to claim 44, further comprising: c. at least one flavoraid.
 46. The mucosal delivery system according to claim 45, wherein the flavoraid is selected from the group consisting of chocolate, white chocolate free of caffeine and theobromine.
 47. A method for reducing the allergenicity of allergens, the method comprising: applying to an allergen source, a solution comprising: a. polysorbate 80 at a concentration ranging from about 0.25% to about 2%; b. an acceptable carrier at a concentration ranging from about 0.1% to about 50%; and c. a non-toxic alcohol at a concentration ranging from about 0.1% to about 50%.
 48. The method according to claim 47, wherein the acceptable carrier is at a concentration ranging from about 0.1% to about 5%.
 49. The method according to claim 47, wherein the acceptable carrier is glycerine.
 50. The method according to claim 47, wherein the non-toxic alcohol is at a concentration ranging from about 0.1% to about 5%.
 51. The method according to claim 47, wherein the non-toxic alcohol is ethyl alcohol or isopropyl alcohol.
 52. The method according to claim 47, further comprising phosphatidylcholine at a concentration ranging from about 0.5% to about 1%; and sodium lauryl sulfate at a concentration ranging from about 0.5% to about 1%.
 53. The method according to claim 47, wherein the allergen source is selected from the group consisting of a poison ivy plant, lipophilic allergenic weed and animal dander.
 54. The method according to claim 47, wherein the reduction in allergenicity is measured using a Bradford assay or ELISA.
 55. The method according to claim 54, wherein there is a reduction in allergenicity of at least 45-fold as measured by the Bradford assay.
 56. The method according to claim 54, wherein there is a reduction in allergenicity of at least 5% as measured by ELISA. 